Cas 229031-94-1,6-benzyloxy-2-(<i>tert</i>-butyl-dimethyl-silanyloxymethyl)-3-methyl-hex-3-enal

229031-94-1

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Basic information

Product Name: 6-benzyloxy-2-(tert-butyl-dimethyl-silanyloxymethyl)-3-methyl-hex-3-enal
Synonyms:
CAS NO:229031-94-1
Molecular Formula:
Molecular Weight: 362.585
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: 6-benzyloxy-2-(tert-butyl-dimethyl-silanyloxymethyl)-3-methyl-hex-3-enal(CAS DataBase Reference)
NIST Chemistry Reference: 6-benzyloxy-2-(tert-butyl-dimethyl-silanyloxymethyl)-3-methyl-hex-3-enal(229031-94-1)
EPA Substance Registry System: 6-benzyloxy-2-(tert-butyl-dimethyl-silanyloxymethyl)-3-methyl-hex-3-enal(229031-94-1)

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: 229031-94-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 229031-94-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,9,0,3 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 229031-94:
(8*2)+(7*2)+(6*9)+(5*0)+(4*3)+(3*1)+(2*9)+(1*4)=121
121 % 10 = 1
So 229031-94-1 is a valid CAS Registry Number.

229031-94-1Upstream product

229031-94-1Downstream Products

229031-94-1Relevant academic research and scientific papers

Rearrangement of epoxides in non-aldol aldol process: Allylic vs. tertiary and secondary carbocationic centers

Jung, Michael E.,Marquez, Rodolfo

, p. 3129 - 3132 (1999)

It has been shown that allylic carbocations are formed in preference to tertiary or secondary carbocations in the rearrangement of substituted epoxides. However protection of the alkene as a bromo ether allows for the desired rearrangement and production of intermediates for the synthesis of the cytotoxic tedanolides.

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