Cas 128806-72-4,Acetic acid 2-hydroxy-5-isopropyl-2-methyl-6-(2-methyl-propenyl)-cyclohexylmethyl ester

128806-72-4

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Basic information

Product Name: Acetic acid 2-hydroxy-5-isopropyl-2-methyl-6-(2-methyl-propenyl)-cyclohexylmethyl ester
Synonyms:
CAS NO:128806-72-4
Molecular Formula:
Molecular Weight: 282.423
EINECS: N/A
Product Categories: N/A
Mol File: 128806-72-4.mol
Article Data: 1

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: Acetic acid 2-hydroxy-5-isopropyl-2-methyl-6-(2-methyl-propenyl)-cyclohexylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid 2-hydroxy-5-isopropyl-2-methyl-6-(2-methyl-propenyl)-cyclohexylmethyl ester(128806-72-4)
EPA Substance Registry System: Acetic acid 2-hydroxy-5-isopropyl-2-methyl-6-(2-methyl-propenyl)-cyclohexylmethyl ester(128806-72-4)

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: 128806-72-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 128806-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,8,0 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 128806-72:
(8*1)+(7*2)+(6*8)+(5*8)+(4*0)+(3*6)+(2*7)+(1*2)=144
144 % 10 = 4
So 128806-72-4 is a valid CAS Registry Number.

128806-72-4Upstream product

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128806-72-4Relevant articles and documents

SYNTHESIS OF BACTERIAL C50 CAROTENOID SARCINAXANTHIN.

Ferezou, J. P.,Julia, M.

, p. 475 - 486 (2007/10/02)

Alkylation of the distal double bond of geranyl acetate 8 with isoprene epoxide 5 has been carried out under anhydrous ZnCl2/nitromethane conditions to give a mixture of C15 hydroxyprenylated compounds.The major diol acetate isomer 12 was dehydrated to the expected γ-cis synthon 17 which was converted into racemic sarcinaxanthin 3 in few steps through the corresponding sulfone 21.

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