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147150-78-5

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147150-78-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147150-78-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,1,5 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 147150-78:
(8*1)+(7*4)+(6*7)+(5*1)+(4*5)+(3*0)+(2*7)+(1*8)=125
125 % 10 = 5
So 147150-78-5 is a valid CAS Registry Number.

147150-78-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chlorosulfonyl-8-fluoro-5-methoxy-[1,2,4]triazolo[1,5-c]pyrimidine

1.2 Other means of identification

Product number -
Other names 2-chlorosulfonyl-5-methoxy-8-fluoro[1,2,4]triazolo[1,5-c]pyrimidine

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:147150-78-5 SDS

147150-78-5Relevant articles and documents

Preparation method of triazolopyrimidine herbicide

-

, (2020/06/20)

The invention belongs to the technical field of organic synthesis, and particularly relates to a preparation method of a triazolopyrimidine herbicide. The preparation method specifically comprises thefollowing steps: a) reacting a compound with the structure represented by formula (I) with thiosemicarbazide, and then isomerizing under an alkaline condition to obtain a compound with the structurerepresented by formula (II); b) carrying out a diazotization reaction on the compound of the formula (II) and sodium nitrite, and then mixing and reacting with sodium hydrogen sulfite and chloride toobtain a compound with the structure represented by formula (III), wherein the chloride comprises copper chloride and/or cuprous chloride; and c) reacting the compound of the formula (III) with a compound with the structure represented by formula (IV) to obtain the triazolopyrimidine herbicide with the structure represented by formula (V). The preparation method provided by the invention has the advantages of mild reaction conditions, low safety risk and good environmental friendliness.

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