Cas 1252016-30-0,5,6-dibenzoyl-11,12-dibromo-1,10-dimethyl-14-thiapentacyclo[8.2.1.1.(3,8)0.(2,9)0.(4,7)]pentadeca-5.11-diene

1252016-30-0

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Basic information

Product Name: 5,6-dibenzoyl-11,12-dibromo-1,10-dimethyl-14-thiapentacyclo[8.2.1.1.(3,8)0.(2,9)0.(4,7)]pentadeca-5.11-diene
Synonyms:
CAS NO:1252016-30-0
Molecular Formula:
Molecular Weight: 596.382
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5,6-dibenzoyl-11,12-dibromo-1,10-dimethyl-14-thiapentacyclo[8.2.1.1.(3,8)0.(2,9)0.(4,7)]pentadeca-5.11-diene(CAS DataBase Reference)
NIST Chemistry Reference: 5,6-dibenzoyl-11,12-dibromo-1,10-dimethyl-14-thiapentacyclo[8.2.1.1.(3,8)0.(2,9)0.(4,7)]pentadeca-5.11-diene(1252016-30-0)
EPA Substance Registry System: 5,6-dibenzoyl-11,12-dibromo-1,10-dimethyl-14-thiapentacyclo[8.2.1.1.(3,8)0.(2,9)0.(4,7)]pentadeca-5.11-diene(1252016-30-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1252016-30-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1252016-30-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,2,0,1 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1252016-30:
(9*1)+(8*2)+(7*5)+(6*2)+(5*0)+(4*1)+(3*6)+(2*3)+(1*0)=100
100 % 10 = 0
So 1252016-30-0 is a valid CAS Registry Number.

1252016-30-0Upstream product

1252031-10-9 5,6-dibenzoyl-11,12-dibromo-1,10-dimethyl-14-thiapentacyclo[8.2.1.1.(3,8)0.(2,9)0.(4,7)]pentadeca-5.11-diene 14-oxide

1252016-30-0Downstream Products

1252016-30-0Relevant academic research and scientific papers

From thiophene S-oxides to 7-thiabicyclo[2.2.1]hept-5-enes

Li, Yuan-Qiang,Thiemann, Carolin,Ohira, Daisuke,Mataka, Shuntaro,Tashiro, Masashi,Thiemann, Thies

experimental part, p. 702 - 704 (2010/03/24)

Oligocycles with a 7-thiabicyclo[2.2.1]hept-5-ene unit have been prepared stereoselectively by cycloaddition of thiophene S-oxides to alkenes and subsequent deoxygenation of the sulfoxy bridge of the cycloadducts with PBr 3.

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