Cas 157358-07-1,Trimethyl-[(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxyethynyl]-silane

157358-07-1

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Basic information

Product Name: Trimethyl-[(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxyethynyl]-silane
Synonyms:
CAS NO:157358-07-1
Molecular Formula:
Molecular Weight: 328.57
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: Trimethyl-[(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxyethynyl]-silane(CAS DataBase Reference)
NIST Chemistry Reference: Trimethyl-[(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxyethynyl]-silane(157358-07-1)
EPA Substance Registry System: Trimethyl-[(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxyethynyl]-silane(157358-07-1)

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: 157358-07-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 157358-07-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,3,5 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 157358-07:
(8*1)+(7*5)+(6*7)+(5*3)+(4*5)+(3*8)+(2*0)+(1*7)=151
151 % 10 = 1
So 157358-07-1 is a valid CAS Registry Number.

157358-07-1Upstream product

157358-07-1Downstream Products

157358-07-1Relevant academic research and scientific papers

A convenient synthesis of hexacarbonyldicobalt complexes of chiral (non-racemic) terminal alkoxyacetylenes

Bernardes, Vania,Verdaguer, Xavier,Moyano, Albert,Pericas, Miquel A.,Riera, Antoni,Greene, Andrew E.

, p. C12 - C14 (2007/10/02)

The hexacarbonyldicobalt complexes of chiral (non-racemic) unsubstituted terminal alkoxyacetylenes have been synthesized for the first time by a novel procedure that involves one-pot transformation of a chiral alcohol to the corresponding trimethylsilylat

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