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36603-29-9

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36603-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36603-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,6,0 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36603-29:
(7*3)+(6*6)+(5*6)+(4*0)+(3*3)+(2*2)+(1*9)=109
109 % 10 = 9
So 36603-29-9 is a valid CAS Registry Number.

36603-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenylhexanenitrile

1.2 Other means of identification

Product number -
Other names 5-phenylhexanonitrile

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:36603-29-9 SDS

36603-29-9Downstream Products

36603-29-9Relevant articles and documents

Cooperative Palladium/Lewis Acid-Catalyzed Transfer Hydrocyanation of Alkenes and Alkynes Using 1-Methylcyclohexa-2,5-diene-1-carbonitrile

Bhunia, Anup,Bergander, Klaus,Studer, Armido

supporting information, p. 16353 - 16359 (2018/11/25)

Catalytic transfer hydrocyanation represents a clean and safe alternative to hydrocyanation processes using toxic HCN gas. Such reactions provide access to pharmaceutically important nitrile derivatives starting with alkenes and alkynes. Herein, an efficient and practical cooperative palladium/Lewis acid-catalyzed transfer hydrocyanation of alkenes and alkynes is presented using 1-methylcyclohexa-2,5-diene-1-carbonitrile as a benign and readily available HCN source. A large set of nitrile derivatives (>50 examples) are prepared from both aliphatic and aromatic alkenes with good to excellent anti-Markovnikov selectivity. A range of aliphatic alkenes engage in selective hydrocyanation to provide the corresponding nitriles. The introduced method is useful for chain walking hydrocyanation of internal alkenes to afford terminal nitriles in good regioselectivities. This protocol is also applicable to late-stage modification of bioactive molecules.

FRIEDEL-CRAFTS ALKYLATION OF BENZENE BY NORMAL ω-CHLOROALKANOIC ACIDS AND THEIR METHYL ESTERS AND NITRILES

Zakharkin, L. I.,Anikina, E. V.

, p. 327 - 330 (2007/10/02)

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