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7-Azabicyclo[4.1.0]heptane-7-carbothioic acid, O-methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71492-65-4

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71492-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71492-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,9 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 71492-65:
(7*7)+(6*1)+(5*4)+(4*9)+(3*2)+(2*6)+(1*5)=134
134 % 10 = 4
So 71492-65-4 is a valid CAS Registry Number.

71492-65-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name O-methyl 7-azabicyclo[4.1.0]heptane-7-carbothioate

1.2 Other means of identification

Product number -
Other names methyl 7-azabicyclo<4.1.0>heptane-7-O-thiocarboxylate

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:71492-65-4 SDS

71492-65-4Downstream Products

71492-65-4Relevant academic research and scientific papers

vic-Iodothiocyanates and Iodoisothiocyanates. Part 3. Further Preperations, and the Formation of 2-Alkoxy-2-thiazolines

Cambie, Richard C.,Chambers, David,Rutledge, Peter S.,Woodgate, Paul D.,Woodgate, Shella D.

, p. 33 - 39 (2007/10/02)

The reactions of (E)-hex-3-ene, 4-t-butylcyclohexene, and 3-t-butylcyclohexene with iodine and potassium thiocyanate are examined.The action of iodine and thiocyanogen with (E)-hex-3-ene gives different results from those reported in the literature.Isomerization of the vic-iodothiocyatates and formation of 2-alkoxy-2-thiazolines from the latter adducts are reported.

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