Cas 100847-62-9,(2E,4E,6E,8E)-3-Methyl-7-trifluoromethyl-9-(2,6,6-trimethyl-cyclohexa-1,3-dienyl)-nona-2,4,6,8-tetraenal

100847-62-9

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Basic information

Product Name: (2E,4E,6E,8E)-3-Methyl-7-trifluoromethyl-9-(2,6,6-trimethyl-cyclohexa-1,3-dienyl)-nona-2,4,6,8-tetraenal
Synonyms:
CAS NO:100847-62-9
Molecular Formula:
Molecular Weight: 336.397
EINECS: N/A
Product Categories: N/A
Mol File: 100847-62-9.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: (2E,4E,6E,8E)-3-Methyl-7-trifluoromethyl-9-(2,6,6-trimethyl-cyclohexa-1,3-dienyl)-nona-2,4,6,8-tetraenal(CAS DataBase Reference)
NIST Chemistry Reference: (2E,4E,6E,8E)-3-Methyl-7-trifluoromethyl-9-(2,6,6-trimethyl-cyclohexa-1,3-dienyl)-nona-2,4,6,8-tetraenal(100847-62-9)
EPA Substance Registry System: (2E,4E,6E,8E)-3-Methyl-7-trifluoromethyl-9-(2,6,6-trimethyl-cyclohexa-1,3-dienyl)-nona-2,4,6,8-tetraenal(100847-62-9)

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: 100847-62-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 100847-62-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,4 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100847-62:
(8*1)+(7*0)+(6*0)+(5*8)+(4*4)+(3*7)+(2*6)+(1*2)=99
99 % 10 = 9
So 100847-62-9 is a valid CAS Registry Number.

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100847-62-9Relevant articles and documents

Fluorinated Retinoids via Crossed Aldol Condensation of 1,1,1-Trifluoroacetone

Mead, Dennis,Loh, Rhonda,Asato, A. E.,Liu, R. S. H.

, p. 2873 - 2876 (2007/10/02)

Piperidine-acetic acid catalyzed crossed aldol condensation of 1,1,1-trifluoroacetone with aryl or α,β-unsaturated aldehydes was found to be a useful method for the preparation of unsaturated trifluoromethyl ketones.Chain extension of these ketones led to several new fluorinated retinoids including the hitherto elusive all-trans isomers of 19,19,19- and 20,20,20-trifluororetinal.

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