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Cbz-D-allo-Ile·DCHA is a chemical compound that combines Cbz-D-allo-Ile, a protected amino acid derivative of isoleucine, with DCHA, a chiral auxiliary utilized in organic synthesis. The carbobenzyloxy (Cbz) group in Cbz-D-allo-Ile shields the carboxyl functionality, enabling selective reactions, while DCHA contributes to the control of stereochemistry in asymmetric synthesis, making the compound a valuable asset for the preparation of complex organic molecules with high selectivity.

253595-73-2

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253595-73-2 Usage

Uses

Used in Pharmaceutical Industry:
Cbz-D-allo-Ile·DCHA is used as a chiral auxiliary and protected amino acid in the synthesis of pharmaceutical compounds for enhancing the selectivity and yield of enantioselective reactions. Its ability to control stereochemistry is crucial for producing single enantiomers of drugs, which can have different biological activities and reduce side effects.
Used in Organic Synthesis:
In the field of organic synthesis, Cbz-D-allo-Ile·DCHA serves as a valuable reagent for the preparation of complex organic molecules with high stereoselectivity. Its use as a chiral auxiliary aids chemists in achieving the desired enantiomeric excess, which is essential for the development of efficient synthetic routes to biologically active compounds.
Used in Asymmetric Catalysis:
Cbz-D-allo-Ile·DCHA is employed as a ligand in asymmetric catalysis to induce chirality in the products of catalytic reactions. This application is vital for the production of enantiomerically pure compounds, which are often required in the synthesis of agrochemicals and pharmaceuticals to ensure optimal biological activity and safety.
Used in Academic Research:
In academic research, Cbz-D-allo-Ile·DCHA is utilized as a model compound to study the effects of chiral auxiliaries on reaction stereochemistry. This research contributes to the understanding of asymmetric synthesis and the development of new methods and catalysts for enantioselective reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 253595-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,5,9 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 253595-73:
(8*2)+(7*5)+(6*3)+(5*5)+(4*9)+(3*5)+(2*7)+(1*3)=162
162 % 10 = 2
So 253595-73-2 is a valid CAS Registry Number.

253595-73-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-cyclohexylcyclohexanamine,(2R,3S)-3-methyl-2-(phenylmethoxycarbonylamino)pentanoic acid

1.2 Other means of identification

Product number -
Other names Z-D-allo-Ile DCHA

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:253595-73-2 SDS

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