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175853-82-4

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175853-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 175853-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,8,5 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 175853-82:
(8*1)+(7*7)+(6*5)+(5*8)+(4*5)+(3*3)+(2*8)+(1*2)=174
174 % 10 = 4
So 175853-82-4 is a valid CAS Registry Number.

175853-82-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-Dihydro-3,5-dimethyl-1,4-oxazin-2-one N-oxide

1.2 Other means of identification

Product number -
Other names 3,5-Dimethyl-4-oxy-5,6-dihydro-[1,4]oxazin-2-one

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:175853-82-4 SDS

175853-82-4Upstream product

175853-82-4Downstream Products

175853-82-4Relevant articles and documents

α-Oximono-esters as precursors to heterocycles - generation of oxazinone N-oxides and cycloaddition to alkene dipolarophiles

Heaney, Frances,Fenlon, Julie,O'Mahony, Colm,McArdle, Patrick,Cunningham, Desmond

, p. 4302 - 4316 (2007/10/03)

Preparation of a series of terminally and internally substituted δ-alkenyl and δ-alkynyl esters 6,7 and 9, potential precursors to oxazin-2-one nitrones, has been attempted. Condensation between pyruvic or benzoylformic acid and the appropriate alcohol pr

Stereochemical control - Nitrones from oximes by 1,3-azaprotio cyclotransfer or 1,2-prototropy

O'Mahony, Colm,Heaney, Frances

, p. 167 - 168 (2007/10/03)

Oximes 1a,b and 10 are configurationally stable at elevated temperatures, the (E)-oximes react exclusively via a concerted 1,3-azaprotio cyclotransfer reaction to give 6- and 7-membered cyclic dipoles, respectively, whilst their Z-isomers react via a 1,2-

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