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5963-60-0

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5963-60-0 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 5963-60-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,6 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5963-60:
(6*5)+(5*9)+(4*6)+(3*3)+(2*6)+(1*0)=120
120 % 10 = 0
So 5963-60-0 is a valid CAS Registry Number.

5963-60-0SDS

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 (2S)-2-amino-5-anilino-5-oxopentanoic acid

1.2 Other means of identification

Product number -
Other names H-GLU(ANILIDE)-OH

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:5963-60-0 SDS

5963-60-0Downstream Products

5963-60-0Relevant articles and documents

A NOVEL THERAPY FOR ERYTHROPOIETIC PROTOPORPHYRIA (EPP) AND X-LINKED PROTOPORPHYRIA (XLP)

-

Paragraph 63; 67, (2020/12/07)

Disclosed are novel compositions and methods of using the same for the treatment of Erythropoiefic protoporphyria (EPP) and X-linked protoporphyria (XLP). Disclosed are methods and compositions related to treating Erythropoietic protoporphyria and X-linked protoporphyria. Also described are therapeutic agents that can inhibit ABCG2. For example, provided herein are therapeutic agents defined by Formula I.

A convenient method of protection and mild deprotection of α-aminoacid group for the synthesis of functional α-aminoacids

Chollet,Miginiac,Rudelle,Bonnemain

, p. 2101 - 2111 (2007/10/02)

Functionalisation of β or γ carboxyl group of aspartic and glutamic acids with labile substituents was performed via the use of N-trichloroethoxycarbonyl-5-oxazolidinone as protective group.

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