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Phenyl[2-phenyl-5-(sulfanylmethyl)-2,3,3a,6a-tetrahydrofuro[2,3-d]isox azol-3-yl]methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77541-42-5

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77541-42-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77541-42-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,5,4 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77541-42:
(7*7)+(6*7)+(5*5)+(4*4)+(3*1)+(2*4)+(1*2)=145
145 % 10 = 5
So 77541-42-5 is a valid CAS Registry Number.

77541-42-5SDS

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-mercaptomethyl-2-phenyl-3-benzoyl-3a,6a-dihydrofuro<3,2-c>isoxazoline

1.2 Other means of identification

Product number -
Other names ((3R,3aS,6aS)-5-Mercaptomethyl-2-phenyl-2,3,3a,6a-tetrahydro-furo[2,3-d]isoxazol-3-yl)-phenyl-methanone

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:77541-42-5 SDS

77541-42-5Downstream Products

77541-42-5Relevant academic research and scientific papers

1,3-DIPOLAR CYCLOADDITION OF C-BENZOYL-N-PHENYLNITRONE WITH FURAN DERIVATIVES. ANOMALOUS DEHYDROGENATION OF CYCLOADDUCTS WITH 2,3-DICHLORO-5,6-DICYANO-1,4-BENZOQUINONE

Fisera, Lubor,Lesko, Jan,Dandarova, Miloslava,Kovac, Jaroslav

, p. 3546 - 3556 (2007/10/02)

C-Benzoyl-N-phenylnitrone reacted with 2-R-substituted (R=phenyl,CH2OH,CH2OCOCH3,CH2SH)furan derivatives at 55 deg C by a 3-dipolar cycloaddition reaction to the unsubstituted furan double bond to give mono- and bisadducts. 2,5-Dimethylfuran afforded monoadduct only.Dehydrogenations of monoadducts of 5-R-2-phenyl-3-benzoyl-3a,6a-dihydrofuroisoxazolines with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone proceeded anomously at 60 deg C: dehydrogenation followed by electrocyclic opening afforded the corresponding ketonitrones.This method of dehydrogenation offersa new preparation of nitrones and further exemplifies the exploitation of products of 1,3-dipolar cycloaddition for synthetic purposes.

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