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(R)-benzyl (2-(cyclohex-1-en-1-yl)-2-(4-methoxyphenyl)ethyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1428475-60-8

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1428475-60-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1428475-60-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,4,7 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1428475-60:
(9*1)+(8*4)+(7*2)+(6*8)+(5*4)+(4*7)+(3*5)+(2*6)+(1*0)=178
178 % 10 = 8
So 1428475-60-8 is a valid CAS Registry Number.

1428475-60-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-benzyl (2-(cyclohex-1-en-1-yl)-2-(4-methoxyphenyl)ethyl)carbamate

1.2 Other means of identification

Product number -
Other names benzyl (R)-(2-(cyclohex-1-en-1-yl)-2-(4-methoxyphenyl)ethyl)carbamate

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:1428475-60-8 SDS

1428475-60-8Relevant academic research and scientific papers

ASYMMETRIC SYNTHESIS OF (-)-VENLAFAXINE USING ORGANOCATALYST

-

, (2015/07/02)

The patent discloses an asymmetric synthesis of (?)-venlafaxine using an organocatalyst via a unified strategy employing organcatalytic Michael addition, regio-selective dehydration and selective epoxide ring opening.

ASYMMETRIC SYNTHESIS OF (-)-VENLAFAXINE USING ORGANOCATALYST

-

, (2014/02/16)

The patent discloses an asymmetric synthesis of (-)-venlafaxine using an organocatalyst via a unified strategy employing organcatalytic Michael addition, regio-selective dehydration and selective epoxide ring opening.

Asymmetric total synthesis of (-)-venlafaxine using an organocatalyst

Chavan, Subhash P.,Garai, Sumanta,Pawar, Kailash P.

, p. 2137 - 2139 (2013/05/21)

An asymmetric total synthesis of (-)-venlafaxine using an organocatalyst has been achieved via a unified strategy employing organcatalytic Michael addition, regio-selective dehydration and selective epoxide ring opening.

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