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2-benzoyloxy-2-(3',4'-methylenedioxyphenyl)-acetonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102034-68-4

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102034-68-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102034-68-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,0,3 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 102034-68:
(8*1)+(7*0)+(6*2)+(5*0)+(4*3)+(3*4)+(2*6)+(1*8)=64
64 % 10 = 4
So 102034-68-4 is a valid CAS Registry Number.

102034-68-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzoyloxy-2-(3',4'-methylenedioxyphenyl)-acetonitrile

1.2 Other means of identification

Product number -
Other names benzo[1,3]dioxol-5-yl-benzoyloxy-acetonitrile

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:102034-68-4 SDS

102034-68-4Relevant academic research and scientific papers

CYANOHYDRINS AS SUBSTRATES IN BENZOIN CONDENSATION. REGIOCONTROLLED MIXED BENZOIN CONDENSATION

Rozwadowska, Maria D.

, p. 3135 - 3140 (2007/10/02)

O-Benzoylated cyanohydrins of aromatic aldehydes have been used as one of the substrates in the benzoin condensation.They were treated with aromatic aldehydes under phase-transfer conditions to result in benzoin benzoates.By this method aldehydes which fail to undergo condensation using traditional conditions could be converted into benzoins.By the Umpolung of reactivity of the pertinent aldehyde it was possible to prepare both isomeric unsymmetrical benzoins, including the thermodynamically less stable ones.

Synthetic entry into the secoisoquinoline alkaloids

Rozwadowska,Chrzanowska

, p. 2885 - 2890 (2007/10/02)

Several analogs of secoisoquinolinc alkaloids bearing a dimethylaminoethyl side chain and a benzilic, or reduced benzilic group were synthesized. Two independent methods based on the intermediacy of 1,3-dithians and O-benzoylated cyanohydrins as acyl anio

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