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6135-51-9

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6135-51-9 Usage

Chemical structure

A compound consisting of a dioxolane ring with a 2-methyl-1,1'-biphenyl group attached to it.

Physical state

Colorless, flammable liquid.

Odor

Faint odor.

Uses

Commonly used as a solvent and as a reagent in organic synthesis.

Applications

Used in the production of pharmaceuticals, agrochemicals, and other organic compounds.

Safety precautions

Should be handled with care due to potential harm if swallowed, inhaled, or absorbed through the skin.

Hazardous effects

Can cause irritation to the eyes and respiratory system.

Handling and storage

Proper safety measures should be taken when handling and storing this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 6135-51-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,3 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6135-51:
(6*6)+(5*1)+(4*3)+(3*5)+(2*5)+(1*1)=79
79 % 10 = 9
So 6135-51-9 is a valid CAS Registry Number.

6135-51-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenylacetophenone ethylene acetal

1.2 Other means of identification

Product number -
Other names 2-p-Biphenyl-2-methyl-dioxolan

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:6135-51-9 SDS

6135-51-9Downstream Products

6135-51-9Relevant articles and documents

The Suzuki-Miyaura Coupling of Nitroarenes

Yadav, M. Ramu,Nagaoka, Masahiro,Kashihara, Myuto,Zhong, Rong-Lin,Miyazaki, Takanori,Sakaki, Shigeyoshi,Nakao, Yoshiaki

supporting information, p. 9423 - 9426 (2017/07/24)

Synthesis of biaryls via the Suzuki-Miyaura coupling (SMC) reaction using nitroarenes as an electrophilic coupling partners is described. Mechanistic studies have revealed that the catalytic cycle of this reaction is initiated by the cleavage of the aryl-nitro (Ar-NO2) bond by palladium, which represents an unprecedented elemental reaction.

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