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Benzaldehyde, 2-(1-phenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61608-90-0

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61608-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61608-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,0 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61608-90:
(7*6)+(6*1)+(5*6)+(4*0)+(3*8)+(2*9)+(1*0)=120
120 % 10 = 0
So 61608-90-0 is a valid CAS Registry Number.

61608-90-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-phenylethyl)benzaldehyde

1.2 Other means of identification

Product number -
Other names -

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:61608-90-0 SDS

61608-90-0Downstream Products

61608-90-0Relevant academic research and scientific papers

Amide-Directed C?H Sodiation by a Sodium Hydride/Iodide Composite

Huang, Yinhua,Chan, Guo Hao,Chiba, Shunsuke

supporting information, p. 6544 - 6547 (2017/05/29)

A new protocol for amide-directed ortho and lateral C?H sodiation is enabled by sodium hydride (NaH) in the presence of either sodium iodide (NaI) or lithium iodide (LiI). The transient organosodium intermediates could be transformed into functionalized aromatic compounds.

Aldimine-directed branched-selective hydroarylation of styrenes

Lee, Pin-Sheng,Yoshikai, Naohiko

supporting information, p. 1240 - 1244 (2013/03/13)

Branching out: A simple and inexpensive cobalt/triarylphosphine catalyst promotes aldimine-directed hydroarylation of styrene with high branched regioselectivity to afford 1,1-diarylethane derivatives in good yields under mild reaction conditions. The ortho-formyl group in the hydroarylation products is amenable to dehydrative cyclization, to give fused polycyclic aromatic hydrocarbons, as well as decarbonylative removal. Copyright

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