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ethyl 3-(chloroformyl)carbazate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15429-42-2

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15429-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15429-42-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,2 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15429-42:
(7*1)+(6*5)+(5*4)+(4*2)+(3*9)+(2*4)+(1*2)=102
102 % 10 = 2
So 15429-42-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H7ClN2O3/c1-2-10-4(9)7-6-3(5)8/h2H2,1H3,(H,6,8)(H,7,9)

15429-42-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-(carbonochloridoylamino)carbamate

1.2 Other means of identification

Product number -
Other names ethyl 2-(chlorocarbonyl)hydrazinecarboxylate

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:15429-42-2 SDS

15429-42-2Relevant academic research and scientific papers

METHOD FOR PRODUCING SEMICARBAZIDE COMPOUND, AND METHOD FOR PRODUCING TRIAZOLIDINEDIONE COMPOUND

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Paragraph 0119-0122; 0127; 0129-0131, (2020/02/14)

PROBLEM TO BE SOLVED: To provide a method for synthesizing a semicarbazide compound which gives the semicarbazide compound without passing through an acyl azide. SOLUTION: Carbonylating agents such as carbonyl diimidazole (CDI) and triphosgene (TCF) are brought into contact with either one of an amine compound and a carbazate compound to form an active intermediate. A semicarbazide compound is synthesized by reacting the resulting active intermediate with the remaining one of the amine compound and the carbazate compound. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

4-Substituted phenyl-1,2,4-triazoline-3,5-diones and their dihydro analogs as analytical reagents

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, (2008/06/13)

A novel reagent useful for preparing adducts of diene so that the diene may be assayed by gas liquid chromatography utilizing an electron capture detection system.

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