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2H-Isoindole-2-acetic acid, 1,3-dihydro-α-[(4-nitrophenyl)methyl]-1,3-dioxo-, ethyl ester is a complex organic compound with the chemical formula C16H13NO6. It is a derivative of isoindole-2-acetic acid, featuring a 1,3-dihydro structure and an α-(4-nitrophenyl)methyl substituent. The molecule contains a 1,3-dioxo group, which is a cyclic ether with two oxygen atoms, and an ethyl ester functional group, indicating the presence of an ester linkage with an ethyl group. 2H-Isoindole-2-aceticacid, 1,3-dihydro-a-[(4-nitrophenyl)methyl]-1,3-dioxo-, ethyl ester is characterized by its potential applications in pharmaceuticals and chemical research, particularly in the synthesis of various biologically active molecules. Its structure provides a foundation for understanding its reactivity and potential interactions within complex chemical systems.

6957-95-5

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6957-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6957-95-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6957-95:
(6*6)+(5*9)+(4*5)+(3*7)+(2*9)+(1*5)=145
145 % 10 = 5
So 6957-95-5 is a valid CAS Registry Number.

6957-95-5SDS

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 4,4'-Dimethyl-4''-nitrophenylamin

1.2 Other means of identification

Product number -
Other names 4-nitro-N,N-phthaloyl-D-phenylalanin-ethyl ester

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:6957-95-5 SDS

6957-95-5Relevant academic research and scientific papers

Melphalan intermediate and preparation method thereof

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Paragraph 0043; 0072; 0077-0078; 0107; 0136; 0141-0142; 0171, (2019/08/02)

The invention discloses a Melphalan intermediate and a preparation method thereof. The Melphalan intermediate is prepared by acidifying a compound p-nitrobenzaldehyde under the action of methanol, a hydrochloric acid solvent, etc. The preparation method has a route with mild reaction conditions, is higher than an existing preparation method in yield, is economical and effective, and is suitable for large-scale industrial production. The synthesis route is as shown in the description.

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