Cas 1338368-41-4,2,6-di-tert-butyl-4-methoxyphenyl 3-methyl-5-(2-(trimethylsilyl)phenyl)hex-5-enoate

1338368-41-4

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Basic information

Product Name: 2,6-di-tert-butyl-4-methoxyphenyl 3-methyl-5-(2-(trimethylsilyl)phenyl)hex-5-enoate
Synonyms: 2,6-di-tert-butyl-4-methoxyphenyl 3-methyl-5-(2-(trimethylsilyl)phenyl)hex-5-enoate
CAS NO:1338368-41-4
Molecular Formula:
Molecular Weight: 494.79
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: 2,6-di-tert-butyl-4-methoxyphenyl 3-methyl-5-(2-(trimethylsilyl)phenyl)hex-5-enoate(CAS DataBase Reference)
NIST Chemistry Reference: 2,6-di-tert-butyl-4-methoxyphenyl 3-methyl-5-(2-(trimethylsilyl)phenyl)hex-5-enoate(1338368-41-4)
EPA Substance Registry System: 2,6-di-tert-butyl-4-methoxyphenyl 3-methyl-5-(2-(trimethylsilyl)phenyl)hex-5-enoate(1338368-41-4)

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: 1338368-41-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1338368-41-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,3,6 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1338368-41:
(9*1)+(8*3)+(7*3)+(6*8)+(5*3)+(4*6)+(3*8)+(2*4)+(1*1)=174
174 % 10 = 4
So 1338368-41-4 is a valid CAS Registry Number.

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1338368-41-4Relevant academic research and scientific papers

Carbon-to-carbon anion relay chemistry: Facile generation of substituted allyllithium species

Zheng, Pinguan,Cai, Zhengxin,Garimallaprabhakaran, Aswinkumar,Rooshenas, Parham,Schreiner, Peter R.,Harmata, Michael

supporting information; experimental part, p. 5255 - 5260 (2011/11/13)

Treatment of [2-(2-bromophenyl)allyl]trimethylsilane with tBuLi in THF at-78 °C resulted in the rapid migration of the trimethylsilyl group to afford an allylic organolithium that can be easily trapped by a wide range of electrophiles. This is a rare exam

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