Cas 1047997-75-0,4-bromo-2-methyl-3-(propan-2-ylidene)-5,5-di-p-tolylpent-4-en-2-ol

1047997-75-0

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Basic information

Product Name: 4-bromo-2-methyl-3-(propan-2-ylidene)-5,5-di-p-tolylpent-4-en-2-ol
Synonyms: 4-bromo-2-methyl-3-(propan-2-ylidene)-5,5-di-p-tolylpent-4-en-2-ol
CAS NO:1047997-75-0
Molecular Formula:
Molecular Weight: 399.371
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: 4-bromo-2-methyl-3-(propan-2-ylidene)-5,5-di-p-tolylpent-4-en-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: 4-bromo-2-methyl-3-(propan-2-ylidene)-5,5-di-p-tolylpent-4-en-2-ol(1047997-75-0)
EPA Substance Registry System: 4-bromo-2-methyl-3-(propan-2-ylidene)-5,5-di-p-tolylpent-4-en-2-ol(1047997-75-0)

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: 1047997-75-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1047997-75-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,7,9,9 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1047997-75:
(9*1)+(8*0)+(7*4)+(6*7)+(5*9)+(4*9)+(3*7)+(2*7)+(1*5)=200
200 % 10 = 0
So 1047997-75-0 is a valid CAS Registry Number.

1047997-75-0Upstream product

331676-35-8 C₂₃H₂₆

1047997-75-0Downstream Products

1047997-97-6 2-methyl-3-(prop-1-en-2-yl)-5,5-di-p-tolylpenta-3,4-dien-2-ol

1047997-75-0Relevant academic research and scientific papers

An efficient method for the synthesis of vinylbromohydrin and vinylbromoalkoxy derivatives and cyclocarbonylation of α-allenic alcohols catalyzed by palladium chloride

Li, Wei,Shi, Min

, p. 6698 - 6705 (2008/12/23)

(Chemical Equation Presented) Vinylidenecyclopropanes undergo hydrobromination or alkoxybromination in the presence of N-bromosuccinimide and water or alcohols to give the corresponding vinylbromohydrin and vinylbromoalkoxy derivatives in moderate to exce

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