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Carbamic acid, [2-cyclohexyl-2-(phenylseleno)ethyl]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106672-52-0

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106672-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106672-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,6,7 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106672-52:
(8*1)+(7*0)+(6*6)+(5*6)+(4*7)+(3*2)+(2*5)+(1*2)=120
120 % 10 = 0
So 106672-52-0 is a valid CAS Registry Number.

106672-52-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl <2-cyclohexyl-2-(phenylseleno)ethyl>carbamate

1.2 Other means of identification

Product number -
Other names (2-Cyclohexyl-2-phenylselanyl-ethyl)-carbamic acid ethyl ester

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:106672-52-0 SDS

106672-52-0Downstream Products

106672-52-0Relevant academic research and scientific papers

Aminoselenenylation of Alkanes: Syntheses of β-Phenylseleno Carbamates and β-Phenylseleno Cyanamides

Francisco, Cosme G.,Hernandez, Rosendo,Leon, Elisa I.,Salazar, Jose A.,Suarez, Ernesto

, p. 2417 - 2427 (2007/10/02)

β-(Phenylseleno)alkylcarbamates and β-(phenylseleno)alkylcyanamides have been synthesized in good yields by reaction of alkenes with carbamates and cyanamide, respectively, in presence of benzeneselenenyl chloride-silver tetrafluoroborate or N-phenylselenophthalimide-H+.The subsequent reductive or oxidative removal of the phenylseleno group affords alkylcarbamates and alkylcyanamides, and allylic carbamates, cyanamides, and cyanimides.

AMINOSELENENYLATION OF OLEFINS. SYNTHESES OF β-PHENYLSELENO CARBAMATES

Francisco, Cosme G.,Leon, Elisa I.,Salazar, Jose A.,Suarez, Ernesto

, p. 2513 - 2516 (2007/10/02)

β-Phenylseleno carbamates have been synthesized by reaction of olefins with phenylselenenyl chloride and carbamates in presence of silver tetrafluoroborate.This reaction constitutes a good method for the conversion of olefins to β-functionalized protected amines.

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