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96988-65-7

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96988-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96988-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,9,8 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96988-65:
(7*9)+(6*6)+(5*9)+(4*8)+(3*8)+(2*6)+(1*5)=217
217 % 10 = 7
So 96988-65-7 is a valid CAS Registry Number.

96988-65-7SDS

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-benzyl-2,3-dihydro-1,4-benzoxazine

1.2 Other means of identification

Product number -
Other names 2H-1,4-Benzoxazine,3,4-dihydro-4-(phenylmethyl)

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:96988-65-7 SDS

96988-65-7Relevant articles and documents

Vinyl selenones: Annulation agents for the synthesis of six-membered benzo-1,4-heterocyclic compounds

Bagnoli, Luana,Casini, Sara,Marini, Francesca,Santi, Claudio,Testaferri, Lorenzo

, p. 481 - 486 (2013/02/23)

A novel and general approach to six-membered bicyclic benzo fused 1,4-heterocycles is described. The addition-cyclization cascade of benzo 1,2-diols, 1,2-thiols and 2-(benzylamino)phenols with stable and easily available vinyl selenones affords differently substituted 2,3-dihydro-1,4- benzodioxines, benzodithiines and 3,4-dihydro-2H-1,4-benzoxazines in good yields. The same procedure has been extended to the synthesis of 1,2,3,4-tetrahydroquinoxalines. All of these heterocycles are present in a variety of biologically active compounds.

Efficient nickel-mediated intramolecular amination of aryl chlorides

Omar-Amrani, Rafik,Thomas, Antoine,Brenner, Eric,Schneider, Raphael,Fort, Yves

, p. 2311 - 2314 (2007/10/03)

(Matrix presented) The use of an in situ generated Ni(0) catalyst associated with 2,2′-bipyridine or N,N′ -bis(2,6-diisopropylphenyl)dihydroimidazol-2-ylidene (SIPr) as a ligand and NaO-t-Bu as the base for the intramolecular coupling of aryl chlorides with amines is described. The procedure has been applied to the formation of five-, six-, and seven-membered rings.

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