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138350-43-3

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138350-43-3 Usage

Chemical Class

Aromatic ketone

Structural Feature

A furan group attached to a phenyl ring

Usage

Flavoring agent in food and beverages

Scent

Sweet and aromatic odor

Application

Fragrance industry for perfumes and scented products

Popularity

Widely used in consumer products due to its pleasant scent and flavor

Check Digit Verification of cas no

The CAS Registry Mumber 138350-43-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,5 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 138350-43:
(8*1)+(7*3)+(6*8)+(5*3)+(4*5)+(3*0)+(2*4)+(1*3)=123
123 % 10 = 3
So 138350-43-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H12O2/c1-9-7-8-13(15-9)12-6-4-3-5-11(12)10(2)14/h3-8H,1-2H3

138350-43-3SDS

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 1-[2-(5-METHYL-2-FURYL)PHENYL]ETHANONE

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:138350-43-3 SDS

138350-43-3Downstream Products

138350-43-3Relevant articles and documents

C-acylation of 2-methylfuran and thiophene using N-acylbenzotriazoles

Katritzky, Alan R.,Suzuki, Kazuyuki,Singh, Sandeep K.

, p. 175 - 178 (2007/10/03)

Reactions of 2-methylfuran and thiophene with readily available N-acylbenzotriazoles (RCOBt, where R = 4-tolyl, 4-methoxyphenyl, benzyl, 4-nitrophenyl, 4-diethylaminophenyl, 2-pyridyl and 1-naphthyl) in the presence of TiCl4 or ZnBr2 produced 2-methyl-4-acylfurans 2a-e and 2-acylthiophenes 3a-f in average yields of 54 % and 75 %, respectively. Literature yields for the preparation of the same compounds are significantly lower.

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