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5-Isothiocyanato-bicyclo[2.2.1]hept-2-ene is a chemical compound with the molecular formula C8H9NS. It is a colorless to pale yellow liquid with a pungent odor. 5-ISOTHIOCYANATO-BICYCLO[2.2.1]HEPT-2-ENE is a derivative of norbornene, a bicyclic hydrocarbon, and features an isothiocyanate functional group. It is used as a building block in the synthesis of various organic compounds, particularly in the preparation of pharmaceuticals and agrochemicals. Due to its reactivity, it is important to handle 5-ISOTHIOCYANATO-BICYCLO[2.2.1]HEPT-2-ENE with care, following appropriate safety measures.

92819-45-9

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92819-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92819-45-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,8,1 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92819-45:
(7*9)+(6*2)+(5*8)+(4*1)+(3*9)+(2*4)+(1*5)=159
159 % 10 = 9
So 92819-45-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NS/c10-5-9-8-4-6-1-2-7(8)3-6/h1-2,6-8H,3-4H2

92819-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-isothiocyanatobicyclo[2.2.1]hept-2-ene

1.2 Other means of identification

Product number -
Other names bicyclo[2.2.1]hept-5-en-2-yl isothiocyanate

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:92819-45-9 SDS

92819-45-9Relevant academic research and scientific papers

ALKYL AND ARYL ISOTHIOCYANATES AS MASKED PRIMARY AMINES

Cho, Cheon-Gyu,Posner, Gary H.

, p. 3599 - 3602 (2007/10/02)

Primary and secondary (but not tertiary) alkyl as well as aryl isothiocyanates react rapidly with 4-methyl-1,2-benzenedithiol (1) in methanol at room temperature, releasing the corresponding amines in good yields.This mild and simple procedure for unmasking amines proceeds chemospecifically with isothiocyanates even in the presence of such normally electrophilic and reactive functionalities as carboxylate ester and N-alkylphthalimide.

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