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13484-51-0

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13484-51-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13484-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,8 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13484-51:
(7*1)+(6*3)+(5*4)+(4*8)+(3*4)+(2*5)+(1*1)=100
100 % 10 = 0
So 13484-51-0 is a valid CAS Registry Number.

13484-51-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5,6-trichloropyrazin-2-amine

1.2 Other means of identification

Product number -
Other names Pyrazinamine,3,5,6-trichloro

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:13484-51-0 SDS

13484-51-0Relevant articles and documents

Nitro derivatives of 2,1,3-benzothiadiazole 1-oxides: synthesis, structural study, and NO release

Konstantinova,Knyazeva,Gatilov, Yu. V.,Zlotin,Rakitin

, p. 95 - 101 (2018)

A convenient one-pot synthesis of nitro derivatives of 2,1,3-benzothiadiazole 1-oxides by the reaction of o-nitroanilines with sulfur monochloride was developed. The structural features of 4-nitrobenzothiadiazole and its N-oxide were considered. High in vitro release of nitric oxide (69%) was found for a 6-nitro-2,1,3-benzothiadiazole sample by the Griess assay, which indicated good prospects for this class of compounds.

Preparation technology of 2-bromo-3,5,6-trichloropyrazine

-

Paragraph 0014-0016; 0024-0026; 0033-0035; 0043; 0044; 0051, (2018/04/21)

The invention discloses a preparation technology of 2-bromo-3,5,6-trichloropyrazine. The preparation technology comprises the following steps of using 2,6-dichloropyrazine as an initiating raw material, and performing ammoniation, halogenation and Sandmeyer reaction, so as to obtain a target compound, namely 2-bromo-3,5,6-trichloropyrazine. The preparation technology has the advantages that by adopting the synthesis route, the obtaining of raw materials is easy, the cost is low, the operation is simple, the product can be easily separated, the selectivity is high, the yield is higher, the total yield can reach 62.7%, and the preparation technology is favorable for actual application.

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