Cas 147102-53-2,2-tert-butyl-7,7-dichloro-4,6-dimethyl-3-oxo-3-phenyl-2-aza-3-phosphabicyclo<4.1.0>hept-4-ene

147102-53-2

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Basic information

Product Name: 2-tert-butyl-7,7-dichloro-4,6-dimethyl-3-oxo-3-phenyl-2-aza-3-phosphabicyclo<4.1.0>hept-4-ene
Synonyms:
CAS NO:147102-53-2
Molecular Formula:
Molecular Weight: 358.248
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: 2-tert-butyl-7,7-dichloro-4,6-dimethyl-3-oxo-3-phenyl-2-aza-3-phosphabicyclo<4.1.0>hept-4-ene(CAS DataBase Reference)
NIST Chemistry Reference: 2-tert-butyl-7,7-dichloro-4,6-dimethyl-3-oxo-3-phenyl-2-aza-3-phosphabicyclo<4.1.0>hept-4-ene(147102-53-2)
EPA Substance Registry System: 2-tert-butyl-7,7-dichloro-4,6-dimethyl-3-oxo-3-phenyl-2-aza-3-phosphabicyclo<4.1.0>hept-4-ene(147102-53-2)

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: 147102-53-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 147102-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,1,0 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 147102-53:
(8*1)+(7*4)+(6*7)+(5*1)+(4*0)+(3*2)+(2*5)+(1*3)=102
102 % 10 = 2
So 147102-53-2 is a valid CAS Registry Number.

147102-53-2Upstream product

147102-52-1 (1R,3S,6S)-2-tert-Butyl-7,7-dichloro-4,6-dimethyl-3-phenyl-2-aza-3-phospha-bicyclo[4.1.0]hept-4-ene

147102-53-2Downstream Products

147102-53-2Relevant academic research and scientific papers

Reaction of dichlorocarbene with 1,2-dihydro 1,2 λ3-azaphosphinine-boranes: Dichlorocyclopropanation and insertion into boron-hydrogen bond

Bedel,Foucaud

, p. 311 - 314 (2007/10/02)

The reaction of dichlorocarbene with 1,2-dihydro 1,2 λ3-azaphosphinine-boranes gave regioselective dichlorocyclopropanation and also insertion of dichlorocarbene into B-H bond. This insertion reaction is general and can be a useful synthetic method for the preparation of functionalized phosphine-boranes.

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