Cas 689296-84-2,1-[(4'S,5'S)-5'-n-hexyl-2',2'-dimethyl-[1,3]-dioxolan-4'-yl]-6-benzyloxyhex-1-ene

689296-84-2

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Basic information

Product Name: 1-[(4'S,5'S)-5'-n-hexyl-2',2'-dimethyl-[1,3]-dioxolan-4'-yl]-6-benzyloxyhex-1-ene
Synonyms: 1-[(4'S,5'S)-5'-n-hexyl-2',2'-dimethyl-[1,3]-dioxolan-4'-yl]-6-benzyloxyhex-1-ene
CAS NO:689296-84-2
Molecular Formula:
Molecular Weight: 374.564
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: 1-[(4'S,5'S)-5'-n-hexyl-2',2'-dimethyl-[1,3]-dioxolan-4'-yl]-6-benzyloxyhex-1-ene(CAS DataBase Reference)
NIST Chemistry Reference: 1-[(4'S,5'S)-5'-n-hexyl-2',2'-dimethyl-[1,3]-dioxolan-4'-yl]-6-benzyloxyhex-1-ene(689296-84-2)
EPA Substance Registry System: 1-[(4'S,5'S)-5'-n-hexyl-2',2'-dimethyl-[1,3]-dioxolan-4'-yl]-6-benzyloxyhex-1-ene(689296-84-2)

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: 689296-84-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 689296-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,9,2,9 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 689296-84:
(8*6)+(7*8)+(6*9)+(5*2)+(4*9)+(3*6)+(2*8)+(1*4)=242
242 % 10 = 2
So 689296-84-2 is a valid CAS Registry Number.

689296-84-2Upstream product

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689296-84-2Relevant academic research and scientific papers

Carbon-carbon bond cleavage by cytochrome P450Biol (CYP107H1)

Cryle, Max J.,De Voss, James J.

, p. 86 - 87 (2004)

Cytochrome P450Biol (CYP107H1) is believed to supply pimelic acid equivalents for biotin biosynthesis in Bacillus subtilis: we report here that the mechanistic pathway adopted by this multifunctional P450 for the in-chain cleavage of fatty acids is via consecutive formation of alcohol and threo-diol intermediates, with the likely absolute configuration of the intermediates also reported.

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