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2-benzoyl-1,2,3,4-tetrahydroisoquinoline-1-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62172-57-0

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62172-57-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62172-57-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,7 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62172-57:
(7*6)+(6*2)+(5*1)+(4*7)+(3*2)+(2*5)+(1*7)=110
110 % 10 = 0
So 62172-57-0 is a valid CAS Registry Number.

62172-57-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzoyl-1,2,3,4-tetrahydroisoquinaldonitrile

1.2 Other means of identification

Product number -
Other names 2-benzoyl-1,2,3,4-tetrahydro-isoquinoline-1-carbonitrile

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:62172-57-0 SDS

62172-57-0Relevant academic research and scientific papers

Mild and highly efficient metal-free oxidative α-cyanation of N-acyl/sulfonyl tetrahydroisoquinolines

Yan, Changcun,Liu, Yuxiu,Wang, Qingmin

, p. 60075 - 60078 (2015/02/19)

A highly efficient metal-free oxidative α-cyanation reaction of N-acyl/sulfonyl tetrahydroisoquinolines under mild conditions was developed. The reaction uses 2,2,6,6-tetramethylpiperidine N-oxide fluoroborate salt (T+BF4-

Protoberberines from Reissert- compounds. Part IX [1]. An alternative approach to dibenzoquinolizine- and isoquinonaphthyridin-13a-carboxylic acids, a novel synthesis of alangimarine

Reimann, Eberhard,Grasberger, Fritz

, p. 193 - 209 (2007/10/03)

3,4-Dihydroisoquinoline-Reissert-compounds were alkylated to 1-benzyl- and 1-picolyl-derivatives, which in turn could selectively be hydrolized yielding various carboxylic acids, among others certain amino acids related to 3′,4′-deoxynorlaudanosoline carboxylic acid (DNLCA). These on treating with ethanolic KOH underwent cyclization to dibenzoquinolizine- and isoquinonaphthyridine-13a-carboxylic acids. Alternatively this cyclization also could be achieved by a more convenient one-pot procedure starting from the same dihydro-Reissert-compounds. Thermal decarboxylation afforded among others the alangia alkaloids alangimarine and dihydroalangimarine. Springer-Verlag 2004.

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.

Organic Sonochemistry. Synthesis and Use of Reissert Compounds under PTC-Ultrasound

Ezquerra, Jesus,Alvarez-Builla, Julio

, p. 917 - 925 (2007/10/02)

Use of phase transfer catalysis and ultrasound stirring improved the synthesis, alkylation and hydrolysis of several Reissert derivatives.

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