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106833-75-4

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106833-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106833-75-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,3 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 106833-75:
(8*1)+(7*0)+(6*6)+(5*8)+(4*3)+(3*3)+(2*7)+(1*5)=124
124 % 10 = 4
So 106833-75-4 is a valid CAS Registry Number.

106833-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-furyl)-1,3-oxazole

1.2 Other means of identification

Product number -
Other names 2-(furyl-2)-oxazole

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:106833-75-4 SDS

106833-75-4Upstream product

106833-75-4Downstream Products

106833-75-4Relevant articles and documents

SYNTHESIS OF 2-ARYL AND 2-HETARYLOXAZOLES FROM THE OXAZOLINES AND OXAZOLIDINES

Belen'kii, L. I.,Cheskis, M. A.,Ryashentseva, M. A.

, p. 650 - 653 (1986)

Treatment of 2-phenyl-, 2-(2-furyl)-, and 2-(2-thienyl)oxazolines with nickel peroxide has been found to give, in addition to the dehydrogenation products (2-substituted oxazoles),the fragmentation products (amides of benzoic, furan-2-carboxylic, and thiophen-2-carboxylic acids).This fragmentation appears to give initially the nitriles, which are then converted into the amides by the nickel peroxide.Catalytic dehydrogenation of 2-phenyloxazoline gives low yields of 2-phenyloxazole, the principal product being benzonitrile.Treatment of the Schiff's bases obtained from ethanolamine and aldehydes (benzaldehyde, furfural, and thiophen-2-aldehyde) with nickel peroxide gives trace amounts of the oxazoles, the principal products being the aldehydes, with smaller amounts of the nitriles.

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