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Hydrazinecarboxylic acid, 2-(2-aminobenzoyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30481-61-9

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30481-61-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30481-61-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,4,8 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30481-61:
(7*3)+(6*0)+(5*4)+(4*8)+(3*1)+(2*6)+(1*1)=89
89 % 10 = 9
So 30481-61-9 is a valid CAS Registry Number.

30481-61-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-[(2-aminobenzoyl)amino]carbamate

1.2 Other means of identification

Product number -
Other names 3-Anthraniloyl-carbazidsaeure-aethylester

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:30481-61-9 SDS

30481-61-9Relevant academic research and scientific papers

HYDRAZIDE COMPOUND AND PESTICIDAL USE OF THE SAME

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Page/Page column 495-496, (2008/06/13)

A hydrazide compound represented by the formula (1): has excellent pesticidal activity.

Reactions of N′-acyl- and N′-tosyl-substituted hydrazides of 2-aminobenzoic acid with carbonyl compounds

Smirnov,Sizova,Luk'yanov,Fedyanin,Antipin

, p. 2444 - 2453 (2007/10/03)

The reactions of N′-acyl and N′-tosyl-substituted hydrazides of 2-aminobenzoic acid with aliphatic, aromatic, and heterocyclic aldehydes or aliphatic ketones afforded 3-acyl- and 3-tosylamido-1,2-dihydroquinazolin-4-one derivatives, respectively. The stru

2,3-Dihydro-5H-thiadiazoloquinazolin-2,5-diones

Gakhar, H. K.,Gupta, Raman,Gill, J. K.

, p. 957 - 959 (2007/10/02)

2,3-Dihydro-5H-thiadiazoloquinazolin-2,5-dione (6) or its 7-methyl derivative has been synthesized by two new convenient routes.In the first approach ethyl 2-(2-aminobenzoyl)hydrazinecarboxylate (3) is used as the starting compound.In the second approach condensation of 3-amino-2-mercaptoquinazolin-4(3H)-one (8) with ethyl chloroformate in the presence of NaOH results in 2-carbethoxy derivative (10) which undergoes cyclisation in refluxing ethyl alcohol to afford 6.The structures have been confirmed on the basis of IR, PMR and analytical data.

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