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87352-10-1

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87352-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87352-10-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,5 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87352-10:
(7*8)+(6*7)+(5*3)+(4*5)+(3*2)+(2*1)+(1*0)=141
141 % 10 = 1
So 87352-10-1 is a valid CAS Registry Number.

87352-10-1SDS

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 methyl 2-methyl-3-phenyl-3H-1,2-oxazole-5-carboxylate

1.2 Other means of identification

Product number -
Other names N-methyl-5-carbomethoxy-3-phenyl-4,5-dehydroisoxazolidine

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:87352-10-1 SDS

87352-10-1Downstream Products

87352-10-1Relevant articles and documents

Thiones as superdipolarophiles. Rates and equilibria of nitrone cycloadditions to thioketones

Huisgen, Rolf,Fisera, Lubor,Giera, Henry,Sustmann, Reiner

, p. 9671 - 9678 (2007/10/02)

1,3-Dipolar cycloadditions of N-methyl-C,C-diphenylnitrone (15) and N-methyl-C-phenylnitrone (16) with aliphatic thioketones are equilibrium reactions. The 1,4,2-oxathiazolidines were characterized and their dissociation constants measured by 1

Benzaldehyde Oxime as a 1,3-Dipole Chameleon

Padwa, Albert,Dent, William,Yeske, Philip E.

, p. 3944 - 3946 (2007/10/02)

Reaction of the iminium salt derived from benzaldehyde oxime and (trimethylsilyl)methyl triflate with cesium fluoride in the presence of electron-dificient alkenes gives rise to azomethine ylide cycloadducts.In sharp contrast, reaction of the salt with alkynes produces dipolar cycloadducts derived from nitrones.

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