What is the 255708-80-6?

255708-80-6 is , while it's Molecular Formula is C3H7N3O3. Used in Pharmaceutical Research and Development: 255708-80-6 is used as a chiral building block for the synthesis of potential drug candidates in the pharmaceutical industry. Its chiral nature allows for the production of enantiomerically pure compounds, which are essential for ensuring the desired therapeutic effects and minimizing potential side effects. Used in the Synthesis of Enantiomerically Pure Compounds: In the field of chiral chemistry, 255708-80-6 is used as a key intermediate for the synthesis of enantiomerically pure compounds. These pure compounds are vital in pharmaceuticals, as they can exhibit different biological activities and potencies compared to their mirror-image counterparts, leading to improved efficacy and reduced side effects. Used in Drug Design and Optimization: 255708-80-6 serves as a versatile component in drug design and optimization processes. Its unique structural features and reactivity enable the development of novel drug candidates with tailored properties, such as improved pharmacokinetics, selectivity, and potency. Used in Medicinal Chemistry: In the realm of medicinal chemistry, 255708-80-6 is employed as a valuable tool for exploring the structure-activity relationships of various biologically active compounds. Its incorporation into different molecular frameworks can provide insights into the design of more effective and safer drugs. Used in Drug Manufacturing Processes: 255708-80-6 is utilized in the manufacturing processes of certain pharmaceuticals, where its unique properties contribute to the production of high-quality, enantiomerically pure drug substances.

What is the CAS number for 255708-80-6?

The CAS number of 255708-80-6 is 255708-80-6.

What is 255708-80-6 (255708-80-6) used for?

255708-80-6, also known as (R)-3-Amino-piperidine-3-carboxylic acid tert-butyl ester, is an organic compound with the molecular formula C11H22N2O2. It is a tert-butyl ester derivative of (R)-3-aminopiperidine-3-carboxylic acid and is commonly used in pharmaceutical research and development, particularly in the synthesis of potential drug candidates. As a chiral compound, it possesses a non-superimposable mirror image, making it valuable in the production of enantiomerically pure compounds, which are often crucial in pharmaceutical applications.

What is the 255708-80-6?

255708-80-6 is , while it's Molecular Formula is C3H7N3O3. Used in Pharmaceutical Research and Development: 255708-80-6 is used as a chiral building block for the synthesis of potential drug candidates in the pharmaceutical industry. Its chiral nature allows for the production of enantiomerically pure compounds, which are essential for ensuring the desired therapeutic effects and minimizing potential side effects. Used in the Synthesis of Enantiomerically Pure Compounds: In the field of chiral chemistry, 255708-80-6 is used as a key intermediate for the synthesis of enantiomerically pure compounds. These pure compounds are vital in pharmaceuticals, as they can exhibit different biological activities and potencies compared to their mirror-image counterparts, leading to improved efficacy and reduced side effects. Used in Drug Design and Optimization: 255708-80-6 serves as a versatile component in drug design and optimization processes. Its unique structural features and reactivity enable the development of novel drug candidates with tailored properties, such as improved pharmacokinetics, selectivity, and potency. Used in Medicinal Chemistry: In the realm of medicinal chemistry, 255708-80-6 is employed as a valuable tool for exploring the structure-activity relationships of various biologically active compounds. Its incorporation into different molecular frameworks can provide insights into the design of more effective and safer drugs. Used in Drug Manufacturing Processes: 255708-80-6 is utilized in the manufacturing processes of certain pharmaceuticals, where its unique properties contribute to the production of high-quality, enantiomerically pure drug substances.

What is the CAS number for 255708-80-6?

The CAS number of 255708-80-6 is 255708-80-6.

What is 255708-80-6 (255708-80-6) used for?

255708-80-6, also known as (R)-3-Amino-piperidine-3-carboxylic acid tert-butyl ester, is an organic compound with the molecular formula C11H22N2O2. It is a tert-butyl ester derivative of (R)-3-aminopiperidine-3-carboxylic acid and is commonly used in pharmaceutical research and development, particularly in the synthesis of potential drug candidates. As a chiral compound, it possesses a non-superimposable mirror image, making it valuable in the production of enantiomerically pure compounds, which are often crucial in pharmaceutical applications.

Your Location：Home >Produts >Pharmaceutical >255708-80-6

Product classification

Contact us

Tel：+86 150 2883 9191

Phone：+86 150 2883 9191

Website：https://www.hbjsztchem.com

Email：admin@cn-chem.com

Address：Room 1805, Block B, Jinyuan Building, Shijiazhuang, Hebei, China

255708-80-6

Product Name：N,O-dimethyl-N'-nitroisourea
Molecular Formula：C3H7N3O3
Specifications：99%
Molecular Weight：133.107

Inquiry

Product Details;

CasNo： 255708-80-6

Molecular Formula： C3H7N3O3

Reliable Quality N,O-dimethyl-N'-nitroisourea 255708-80-6 Hot Sale with Chinese Manufacturer

Molecular Formula:C3H7N3O3
Molecular Weight:133.107
PSA：79.44000
LogP:0.31400

255708-80-6 Relevant articles

A synthetic method of the dinotefuran (by machine translation)

-

Paragraph 0057; 0059; 0076; 0077; 0095; 0097, (2017/08/27)

The invention discloses a method for syn...

N, O - dimethyl - N - nitro-isourea preparation method

-

Paragraph 0021; 0022; 0023; 0024; 0025; 0026; 0027-0042, (2017/08/24)

The invention discloses a method for pre...

IMPROVED METHOD FOR PRODUCING NITROISOUREA DERIVATIVE

-

Page/Page column 4-5, (2008/12/04)

Disclosed is an improved process for pro...

255708-80-6 Process route

: 57538-27-9
O-methyl-N-nitroisourea

: 74-89-5
methylamine

: 255708-80-6
N,O-dimethyl-N'-nitroisourea

Conditions

Conditions	Yield
With hydrogenchloride; sodium chloride; In water; at 40 ℃; for 6h;	95%

: C₄H₁₂N₂O₅S

: 255708-80-6
N,O-dimethyl-N'-nitroisourea

Conditions

Conditions	Yield
With sulfuric acid; nitric acid; at 25 ℃; Concentration;	43.9 g

255708-80-6 Upstream products

57538-27-9
O-methyl-N-nitroisourea
593-51-1
methylamine hydrochloride
57538-27-9
O-methyl-N-nitroisourea
74-89-5
methylamine

Relevant Products

HATU
CAS：148893-10-1
N-Phenylglycine
CAS：103-01-5
2-Chloro-5-fluoropyrimidine
CAS：62802-42-0

Home

About us

Produts

pharmaceutical intermediates

dye intermediates

detergent raw material

cosmetics raw materials and chemical reagents

Pharmaceutical

Adhesive and Sealant

Agrochemicals

Catalyst and Auxiliary

Organic Chemicals

Synthetic Flavours & Fragrances

News

Contact Us