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9,10-dioxa-anti-(methyl,methyl)(methy,bromo)bimane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79746-51-3

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79746-51-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79746-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,4 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79746-51:
(7*7)+(6*9)+(5*7)+(4*4)+(3*6)+(2*5)+(1*1)=183
183 % 10 = 3
So 79746-51-3 is a valid CAS Registry Number.

79746-51-3SDS

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 9,10-dioxa-anti-(methyl,methyl)(methy,bromo)bimane

1.2 Other means of identification

Product number -
Other names -

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:79746-51-3 SDS

79746-51-3Downstream Products

79746-51-3Relevant academic research and scientific papers

Bimanes. 10. Photochemical Rearrangement of 1,5-Diazabicycloocta-3,7-diene-2,6-diones (9,10-Dioxa-anti-bimanes)

Kanety, Hannah,Dodiuk, Hanna,Kosower, Edward M.

, p. 207 - 213 (1982)

1,5-Diazabicycloocta-3,7-diene-2,6-diones (9,10-dioxa-anti-bimanes) rearrange quantitatively on irradiation in the 320 nm absorption band to isomeric lactones, one from symmetrical bimanes and two from unsymmetrical bimanes ("mixed" bimanes).The quantum yield of lactone is often high and depends upon bimane substitution and solvent viscosity.Fast intersystem crossing (Huppert et al.), oxygen inhibition of lactone formation, and efficient formation of lactone via a triplet sensitizer implicate the triplet as a key intermediate.The suggested mechanism of lactoneformation involves a twisted ?-?* triplet.

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