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78387-30-1

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78387-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78387-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,3,8 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78387-30:
(7*7)+(6*8)+(5*3)+(4*8)+(3*7)+(2*3)+(1*0)=171
171 % 10 = 1
So 78387-30-1 is a valid CAS Registry Number.

78387-30-1SDS

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 methyl N-[3-acetyl-4-(2,4-dioxopentan-3-yl)-2-methylpyrrol-1-yl]carbamate

1.2 Other means of identification

Product number -
Other names -

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:78387-30-1 SDS

78387-30-1Downstream Products

78387-30-1Relevant articles and documents

Addition and Cycloaddition Reactions of β-Chloroazo-olefins

Gilchrist, Thomas L.,Stevens, John A.,Parton, Brian

, p. 1741 - 1746 (2007/10/02)

2-Chloro-1-(2,4-dinitrophenylazo)ethene (1a) has been isolated, and the corresponding alkoxycarbonylazo compounds (1b) and (1c) have been generated in solution, as the first examples of azo-olefins bearing single β-halogeno substituents.The compounds (1a) and (1b) undergo cycloaddition to indene and to ethyl vinyl ether with high endo stereoselectivity.Furan and cyclopentadiene give the cycloadducts (6) and (7), respectively, with (1a).Nucleophilic addition-elimination reactions are observed with piperidine, indole, thiophenol, and carbanions.In most of these reactions the primary products are subject to further nucleophilic attack: thus, the hydrazones (11) formed by addition of carbanions are converted into aminopyrroles (12) by further reaction with the carbanions and dehydration.

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