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Benzaldehyde, 4-chloro-2-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81992-91-8

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81992-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81992-91-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,9,9 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81992-91:
(7*8)+(6*1)+(5*9)+(4*9)+(3*2)+(2*9)+(1*1)=168
168 % 10 = 8
So 81992-91-8 is a valid CAS Registry Number.

81992-91-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-4-chlorobenzaldehyde

1.2 Other means of identification

Product number -
Other names Benzaldehyde,4-chloro-2-(phenylmethyl)

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:81992-91-8 SDS

81992-91-8Relevant academic research and scientific papers

Palladium-catalyzed benzylic C(sp3)–H arylation of o-alkylbenzaldehydes

Lei, Lan,Wu, Ping,Liu, Zhuqing,Lou, Jiang

supporting information, (2021/02/16)

The palladium-catalyzed benzylic C(sp3)–H arylation of o-alkylbenzaldehyde derivatives was achieved utilizing 2-dimethylaminoethylamine as a novel transient directing group. The γ-C(sp3)–H arylation reaction efficiently afforded a variety of arylated o-alkylbenzaldehydes and polycyclic aromatic hydrocarbons (PAHs) in one pot, exhibiting high functional group tolerance with broad substrate scope. The aliphatic diamine auxiliary represents a simple, inexpensive, readily available, and removable directing group for C–H activation. The resultant o-benzylbenzaldehyde products could be diversely transformed into potentially important synthetic intermediates under mild conditions.

Pyrrolo[3,4-d][2]benzazepinones

-

, (2008/06/13)

The present invention relates to compounds of the formula STR1 wherein R1 and R3 are selected from the group consisting of hydrogen, lower alkyl, hydroxy, lower alkoxy or acyloxy and R2 and R4 are hydrogen or R

2-Benzazepines. 2. Thiazolobenzazepines

Benjamin, Louis E.,Fryer, R. Ian,Gilman, Norman W.,Trybulski, Eugene J.

, p. 100 - 103 (2007/10/02)

As part of a program in the area of annelated 2-benzazepines, several thiazolobenzazepines were prepared.Treatment of the bromo ketones 7-9 with various thio amides gave the thiazoles 10-15, which when treated with methylamine gave the title com

Pyrazolobenzazepines

-

, (2008/06/13)

There are presented compounds of the formulas STR1 wherein R1 is hydrogen or lower alkyl; R2 and R3 are selected from the group consisting of hydrogen, lower alkyl, C2 to C7 carboxylic acids, hydroxy

Pyrrolo[3,4-d][2]benzazepines

-

, (2008/06/13)

The present invention relates to compounds of the formula STR1 wherein R1 is selected from the group consisting of hydrogen, lower alkyl, C3 to C7 alkenyl or alkynyl, hydroxymethyl, the group STR2 wherein R11 is

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