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51534-05-5

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51534-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51534-05-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,3 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51534-05:
(7*5)+(6*1)+(5*5)+(4*3)+(3*4)+(2*0)+(1*5)=95
95 % 10 = 5
So 51534-05-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H10N2O2/c1-8-4(6)3-5(7)9-2/h6-7H,3H2,1-2H3/b6-4-,7-5-

51534-05-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1t,3-bis-methylsulfanyl-dec-1-ene

1.2 Other means of identification

Product number -
Other names 1,3-Bis(methylthio)-1-decen

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:51534-05-5 SDS

51534-05-5Relevant articles and documents

Preparation method of 2-amino-4,6-dimethoxypyrimidine

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Paragraph 0030-0031; 0035-0036; 0040-0041; 0045-0046; 0050-, (2020/04/02)

A preparation method of 2-amino-4,6-diamino-1,3,4-triazole comprises the following steps: malononitrile and methanol which are used as raw materials undergo a hydrogen chloride aeration reaction in asolvent which is one of methylbenzene, dimethylbenzene, chlorobenzene and dichloroethane to generate 1,3-dimethoxypropylenediamine dihydrochloride, a water-insoluble quaternary amine organic alkali isdropwise added into the obtained reaction system without filtration or other post-treatment operations in order to regulate the pH value of the reaction system to 6-8, a cyanamide solid is added, a reaction is performed to generate 3-amino-3-methoxy-N-nitrile-2-propylamidine, and the 3-amino-3-methoxy-N-nitrile-2-propylamidine is heated to react to generate the 2-amino-4,6-dimethoxypyrimidine product. The method for preparing the 2-amino-4,6-dimethoxypyrimidine by using a one-pot process has the advantages of mild reaction conditions, safety, environmental friendliness, process operation simplification, and small amount of three wastes, makes the total synthesis yield of the four-step reaction reach 80% or above and the product content reach 99% or above, and is suitable for green industrial production.

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