Cas 191939-01-2,(3Z,7E)-4-Iodo-8-methyl-1-(5-triethylsilanyl-furan-3-yl)-10-(2,6,6-trimethyl-cyclohex-1-enyl)-deca-3,7-dien-1-ol

191939-01-2

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Basic information

Product Name: (3Z,7E)-4-Iodo-8-methyl-1-(5-triethylsilanyl-furan-3-yl)-10-(2,6,6-trimethyl-cyclohex-1-enyl)-deca-3,7-dien-1-ol
Synonyms: (3Z,7E)-4-Iodo-8-methyl-1-(5-triethylsilanyl-furan-3-yl)-10-(2,6,6-trimethyl-cyclohex-1-enyl)-deca-3,7-dien-1-ol
CAS NO:191939-01-2
Molecular Formula:
Molecular Weight: 596.708
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: (3Z,7E)-4-Iodo-8-methyl-1-(5-triethylsilanyl-furan-3-yl)-10-(2,6,6-trimethyl-cyclohex-1-enyl)-deca-3,7-dien-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: (3Z,7E)-4-Iodo-8-methyl-1-(5-triethylsilanyl-furan-3-yl)-10-(2,6,6-trimethyl-cyclohex-1-enyl)-deca-3,7-dien-1-ol(191939-01-2)
EPA Substance Registry System: (3Z,7E)-4-Iodo-8-methyl-1-(5-triethylsilanyl-furan-3-yl)-10-(2,6,6-trimethyl-cyclohex-1-enyl)-deca-3,7-dien-1-ol(191939-01-2)

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: 191939-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 191939-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,9,3 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 191939-01:
(8*1)+(7*9)+(6*1)+(5*9)+(4*3)+(3*9)+(2*0)+(1*1)=162
162 % 10 = 2
So 191939-01-2 is a valid CAS Registry Number.

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191939-01-2Relevant academic research and scientific papers

Synthesis of manoalide using a 1,2-metallate rearrangement

Pommier, Agnes,Kocienski, Philip J.

, p. 1139 - 1140 (1997)

Manoalide, a marine antiinflammatory sesterterpenoid, has been synthesised using a 1,2-metallate rearrangement of a higher order cuprate and a Pd0-catalysed carbonylation of an iodo alkene to generate the central dihydropyranone ring.

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