CAS 361440-67-7 Purity >98.5% (HPLC) Factory

Short Description:

(1S,3S,5S)-3-(Aminocarbonyl)-2-Azabicyclo [3.1.0]hexane-2-Carboxylic Acid tert-Butyl Ester 

CAS: 361440-67-7

Purity: >98.5% (HPLC) 

Appearance: White Powder

Intermediate of API (CAS: 361442-04-8)

E-Mail: alvin@ruifuchem.com


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Description:

Chemical Properties:

Chemical Name (1S,3S,5S)-3-(Aminocarbonyl)-2-Azabicyclo[3.1.0]hexane-2-Carboxylic Acid tert-Butyl Ester
Synonyms N-Boc-L-cis-4,5-Methanoprolineamide; N-Boc-cis-4,5-Methano-L-Prolinamide; tert-Butyl (1S,3S,5S)-3-Carbamoyl-2-Azabicyclo[3.1.0]hexane-2-Carboxylate
CAS Number 361440-67-7
CAT Number RF-PI1990
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C11H18N2O3
Molecular Weight 226.27
Boiling Point  388.9±21.0℃
Density 1.228
Brand Ruifu Chemical

Specifications:

Item Specifications
Appearance White Powder
Purity / Analysis Method >98.5% (HPLC)
Loss on Drying <0.50%
Residue on Ignition <0.20%
Individual Impurities <1.00%
Total Impurities <1.50%
Test Standard Enterprise Standard
Usage Intermediate of API (CAS: 361442-04-8)

Package & Storage:

Package: Bottle, Aluminium foil bag, 25kg/Cardboard Drum, or according to customer's requirement

Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moisture

Advantages:

1

FAQ:

Application:

(1S,3S,5S)-3-(Aminocarbonyl)-2-Azabicyclo[3.1.0]hexane-2-Carboxylic Acid tert-Butyl Ester (CAS: 361440-67-7) is an intermediate of API (CAS: 361442-04-8). (CAS: 361442-04-8) is an oral hypoglycemic (anti-diabetic drug) of the dipeptidyl peptidase-4 (DPP-4) inhibitor class of drugs. Early development was solely by Bristol-Myers Squibb; in 2007 AstraZeneca joined with Bristol-Myers Squibb to co-develop the final compound and collaborate on the marketing of the drug. In June 2008, it was announced that Onglyza would be the trade name under which will be marketed. API (CAS: 361442-04-8) is used as monotherapy or in combination with other drugs for the treatment of type 2 diabetes. It is absorbed rapidly after oral administration and has a pharmacokinetic profile compatible with once daily dosing. It plays the role through inhibiting GLP-l degradation. GLP-I is the hormones naturally produced in the intestine after taking food.

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