Cas 77086-42-1,2-[4-(4-Chloro-phenyl)-3-trimethylsilanyloxy-cyclohex-2-enyl]-propionic acid methyl ester

77086-42-1

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Basic information

Product Name: 2-[4-(4-Chloro-phenyl)-3-trimethylsilanyloxy-cyclohex-2-enyl]-propionic acid methyl ester
Synonyms: 2-[4-(4-Chloro-phenyl)-3-trimethylsilanyloxy-cyclohex-2-enyl]-propionic acid methyl ester
CAS NO:77086-42-1
Molecular Formula:
Molecular Weight: 366.96
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-[4-(4-Chloro-phenyl)-3-trimethylsilanyloxy-cyclohex-2-enyl]-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[4-(4-Chloro-phenyl)-3-trimethylsilanyloxy-cyclohex-2-enyl]-propionic acid methyl ester(77086-42-1)
EPA Substance Registry System: 2-[4-(4-Chloro-phenyl)-3-trimethylsilanyloxy-cyclohex-2-enyl]-propionic acid methyl ester(77086-42-1)

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: 77086-42-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 77086-42-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,8 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77086-42:
(7*7)+(6*7)+(5*0)+(4*8)+(3*6)+(2*4)+(1*2)=151
151 % 10 = 1
So 77086-42-1 is a valid CAS Registry Number.

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77086-42-1Relevant academic research and scientific papers

O-silylated ketene acetal chemistry; β-(alkoxycarbonyl)methyl O-silyl enolates, useful synthons for α-substituted-β-(alkoxycarbonyl)methylalkanones

Kita,Segawa,Haruta,Fujii,Tamura

, p. 3779 - 3782 (2007/10/02)

Conjugate addition of O-silylated ketene acetals 2 to α,β-unsaturated carbonyl compounds 1 in acetonitrile gave quantitative yields of the corresponding β-(alkoxycarbonyl)methyl O-silyl enolates 4. Site specific electrophilic substitutions of 4 yielded th

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