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24537-38-0

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24537-38-0 Usage

Physical state

Colorless liquid

Usage

Reagent in organic synthesis

Applications

a. Production of pharmaceuticals
b. Production of agrochemicals
c. Production of dyes

Role

Precursor in the synthesis of various organic compounds

Safety

Generally considered safe when handled and used properly

Precaution

Potential toxicity; should be handled with caution

Check Digit Verification of cas no

The CAS Registry Mumber 24537-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,3 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24537-38:
(7*2)+(6*4)+(5*5)+(4*3)+(3*7)+(2*3)+(1*8)=110
110 % 10 = 0
So 24537-38-0 is a valid CAS Registry Number.

24537-38-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(methoxycarbonylamino)carbamate

1.2 Other means of identification

Product number -
Other names 1,2-Hydrazinedicarboxylicacid,1,1-dimethylethyl methyl ester (9CI)

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:24537-38-0 SDS

24537-38-0Downstream Products

24537-38-0Relevant articles and documents

Enantioselective α-amination of 1,3-dicarbonyl compounds using squaramide derivatives as hydrogen bonding catalysts

Konishi, Hideyuki,Lam, Tin Yiu,Malerich, Jeremiah P.,Rawal, Viresh H.

supporting information; experimental part, p. 2028 - 2031 (2010/06/21)

Figure presented Catalytic enantioselective α-hydrazination of 1,3-dicarbonyl compounds with azodicarboxylates was investigated in the presence of our newly developed hydrogen bonding catalyst, squaramide 3j. High yields and high enantioselectivities were

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