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Thiocyanic acid, (1R,4R)-3,3-dimethyl-2-methylenebicyclo[2.2.1]hept-1-yl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

521068-33-7

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521068-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 521068-33-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,1,0,6 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 521068-33:
(8*5)+(7*2)+(6*1)+(5*0)+(4*6)+(3*8)+(2*3)+(1*3)=117
117 % 10 = 7
So 521068-33-7 is a valid CAS Registry Number.

521068-33-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [(1R,4R)-2,2-dimethyl-3-methylidene-4-bicyclo[2.2.1]heptanyl] thiocyanate

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:521068-33-7 SDS

521068-33-7Downstream Products

521068-33-7Relevant academic research and scientific papers

A novel and simple procedure for the enantiospecific synthesis of bridgehead norbornane thioethers and thiocyanates

Garcia Martinez, Antonio,Teso Vilar, Enrique,Moreno Jimenez, Florencio,Alvarez Garcia, Ana Maria,Pinilla Rodriguez, Patricia

, p. 2635 - 2639 (2007/10/03)

An easy three-step route for the enantiospecific synthesis of novel 1-norbornyl thioethers and thiocyanates from readily available natural fenchone and camphor is described. The key step of the synthetic route is the nucleophilic substitution over the sulfenyl sulfur atom of the intermediate thiotriflates by the corresponding C-nucleophiles.

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