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791625-59-7

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791625-59-7 Usage

General Description

BOC-D-2,4-DIMETHYLPHE is a chemical compound with the molecular formula C16H23NO5. It is a derivative of 2,4-dimethylphenol and contains a BOC (tert-butyloxycarbonyl) protecting group. BOC-D-2,4-DIMETHYLPHE is commonly used as a building block in organic synthesis and peptide chemistry. The BOC protecting group can be removed under acidic conditions, allowing for the selective reaction of the 2,4-dimethylphenol moiety. BOC-D-2,4-DIMETHYLPHE is a versatile and important intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 791625-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,1,6,2 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 791625-59:
(8*7)+(7*9)+(6*1)+(5*6)+(4*2)+(3*5)+(2*5)+(1*9)=197
197 % 10 = 7
So 791625-59-7 is a valid CAS Registry Number.

791625-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-3-(2,4-dimethylphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid

1.2 Other means of identification

Product number -
Other names BOC-D-2,4-DIMETHYLPHE

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:791625-59-7 SDS

791625-59-7Downstream Products

791625-59-7Relevant articles and documents

Asymmetric synthesis of all six regioisomers of N-boc-dimethylphenylalanines

Ouchi, Hidekazu,Kumagai, Midori,Sakurada, Shinobu,Takahata, Hiroki

, p. 505 - 514 (2007/10/03)

All possible regioisomers of dimethyl-substituted (S)-phenylalanine were efficiently synthesized by reacting the Ni(II)-complex of the chiral Schiff base of glycine with (S)-2-N-(N-benzylprolyl)-aminobenzophenone.

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