Cas 86342-81-6,(6E,14E)-2,6,10,11,15,19-Hexamethyl-10,11-divinyl-icosa-2,6,14,18-tetraene

86342-81-6

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Basic information

Product Name: (6E,14E)-2,6,10,11,15,19-Hexamethyl-10,11-divinyl-icosa-2,6,14,18-tetraene
Synonyms: (6E,14E)-2,6,10,11,15,19-Hexamethyl-10,11-divinyl-icosa-2,6,14,18-tetraene
CAS NO:86342-81-6
Molecular Formula:
Molecular Weight: 410.727
EINECS: N/A
Product Categories: N/A
Mol File: 86342-81-6.mol
Article Data: 2

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: (6E,14E)-2,6,10,11,15,19-Hexamethyl-10,11-divinyl-icosa-2,6,14,18-tetraene(CAS DataBase Reference)
NIST Chemistry Reference: (6E,14E)-2,6,10,11,15,19-Hexamethyl-10,11-divinyl-icosa-2,6,14,18-tetraene(86342-81-6)
EPA Substance Registry System: (6E,14E)-2,6,10,11,15,19-Hexamethyl-10,11-divinyl-icosa-2,6,14,18-tetraene(86342-81-6)

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: 86342-81-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 86342-81-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,3,4 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 86342-81:
(7*8)+(6*6)+(5*3)+(4*4)+(3*2)+(2*8)+(1*1)=146
146 % 10 = 6
So 86342-81-6 is a valid CAS Registry Number.

86342-81-6Upstream product

24163-93-7 farnesyl bromide

86342-81-6Downstream Products

86342-81-6Relevant articles and documents

REDUCTIVE COUPLING OF ALLYLIC HALIDES BY CHLOROTRIS(TRIPHENYLPHOSPHINE)COBALT(I)

Momose, Den-ichi,Iguchi, Kazuo,Sugiyama, Toshikazu,Yamada, Yasuji

, p. 921 - 924 (1983)

Reactions of geranyl and farnesyl halide, and their geometrical isomers with chlorotris(triphenylphosphine)cobalt(I) gave the corresponding geometrically pure coupling products under mild and non-basic conditions.Squalenes were stereospecifically synthesized by this method.

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