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171754-03-3

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171754-03-3 Usage

General Description

2-Azabicyclo[2.2.1]heptane-3-carboxylic acid, (1S,3R,4R)- is a chemical compound categorized as a bicyclic amino acid. It contains a ring structure with a nitrogen atom, making it a heterocyclic compound. This chemical is important in the field of pharmaceuticals as it is a precursor in the synthesis of various drugs and pharmaceuticals, particularly in the production of antibiotics. Its unique structure and properties make it a key component in the development of new pharmaceutical products.

Check Digit Verification of cas no

The CAS Registry Mumber 171754-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,7,5 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 171754-03:
(8*1)+(7*7)+(6*1)+(5*7)+(4*5)+(3*4)+(2*0)+(1*3)=133
133 % 10 = 3
So 171754-03-3 is a valid CAS Registry Number.

171754-03-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,3R,4R)-2-aza-bicyclo-[2.2.1]-heptane-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names (1S,3R,4R)-2-azabicyclo[2.2.1]heptane-3-carboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:171754-03-3 SDS

171754-03-3Downstream Products

171754-03-3Relevant articles and documents

Synthesis of fragments of transforming growth factor alpha incorporating exo-2-azabicyclo[2,2,1 ]heptane-3-carboxylic acids as proline substitutes

Mellor, John M.

, p. 6765 - 6768 (1995)

Two novel amino acids, the enantiomers ofexo 2-azabicyclo [2,2,1]heptane-3-carboxylic acid have been independent synthesized by the aza Diels Alder reaction using a chiral auxiliary. The two acids have been advanced via solid phase synthesis to afford linear sequences, which have been cyclized to afford cyclic disulfide peptides, analogues of fragments of TGFd. The structures of these and other fragments have been firmly established.

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