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10174-83-1

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10174-83-1 Usage

Chemical Properties

white crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 10174-83-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,7 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10174-83:
(7*1)+(6*0)+(5*1)+(4*7)+(3*4)+(2*8)+(1*3)=71
71 % 10 = 1
So 10174-83-1 is a valid CAS Registry Number.
InChI:InChI=1/C19H18N2O3/c1-23-17-10-14-8-9-21(19(22)13-6-4-3-5-7-13)16(12-20)15(14)11-18(17)24-2/h3-7,10-11,16H,8-9H2,1-2H3/t16-/m0/s1

10174-83-1SDS

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 2-Benzoyl-1-cyano-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

1.2 Other means of identification

Product number -
Other names 2-Benzoyl-6,7-dimethoxy-1,2,3,4-tetrahydroisochinaldonitril

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:10174-83-1 SDS

10174-83-1Relevant articles and documents

DDQ-promoted mild and efficient metal-free oxidative α-cyanation of N-acyl/sulfonyl 1,2,3,4-tetrahydroisoquinolines

Kim, Hong Pyo,Yu, Heesun,Kim, Hyoungsu,Kim, Seok-Ho,Lee, Dongjoo

, (2018)

A mild and highly efficient metal-free oxidative α-cyanation of N-acyl/sulfonyl 1,2,3,4-tetrahydroisoquinolines (THIQs) has been accomplished at an ambient temperature via DDQ oxidation and subsequent trapping of N-acyl/sulfonyl iminium ions with (n-Bu)s

IMPROVED SYNTHESIS OF DIHYDROISOQUINOLINE REISSERT COMPOUNDS

Jackson, Yvette A.,Stephenson, E. Kyle,Cava, Michael P.

, p. 1047 - 1050 (2007/10/02)

Conversion of a series of 3,4-dihydroisoquinolines to their corresponding Reissert compounds was improved significantly over the usual reaction conditions by buffering the reaction medium at pH 8.

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