Cas 1158483-01-2,(+)-(R)-1-(4-tert-butylphenyl)-2-(1-trityl-1H-imidazol-4-yl)ethanol

1158483-01-2

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Basic information

Product Name: (+)-(R)-1-(4-tert-butylphenyl)-2-(1-trityl-1H-imidazol-4-yl)ethanol
Synonyms: (+)-(R)-1-(4-tert-butylphenyl)-2-(1-trityl-1H-imidazol-4-yl)ethanol
CAS NO:1158483-01-2
Molecular Formula:
Molecular Weight: 486.657
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: (+)-(R)-1-(4-tert-butylphenyl)-2-(1-trityl-1H-imidazol-4-yl)ethanol(CAS DataBase Reference)
NIST Chemistry Reference: (+)-(R)-1-(4-tert-butylphenyl)-2-(1-trityl-1H-imidazol-4-yl)ethanol(1158483-01-2)
EPA Substance Registry System: (+)-(R)-1-(4-tert-butylphenyl)-2-(1-trityl-1H-imidazol-4-yl)ethanol(1158483-01-2)

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: 1158483-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1158483-01-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,8,4,8 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1158483-01:
(9*1)+(8*1)+(7*5)+(6*8)+(5*4)+(4*8)+(3*3)+(2*0)+(1*1)=162
162 % 10 = 2
So 1158483-01-2 is a valid CAS Registry Number.

1158483-01-2Upstream product

1158482-96-2 (+)-(R)-4-[2-allyloxy-2-(4-tert-butylphenyl)ethyl]-1-trityl-1H-imidazole

1158483-01-2Downstream Products

1158483-01-2Relevant academic research and scientific papers

Synthesis of enantioenriched secondary and tertiary alcohols via tricarbonylchromium(0) complexes of benzyl allyl ethers

Abecassis, Keren,Gibson, Susan E.,Martin-Fontecha, Mar

, p. 1606 - 1611 (2009)

Allyl ethers of the tricarbonylchromium(0) complexes of benzylic alcohols undergo highly enanlioselective benzylic funclionalisation using a chiral base/electrophilic quench sequence; the allyl group is readily removed to reveal a hydroxy group as demonst

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