Cas 431990-36-2,2-[(1RS,4E,6E)-10-(tert-butyldimethylsilanyloxy)-1-(tert-butyldiphenylsilanyloxy)-4-methyldeca-4,6-dienyl]thiophene

431990-36-2

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Basic information

Product Name: 2-[(1RS,4E,6E)-10-(tert-butyldimethylsilanyloxy)-1-(tert-butyldiphenylsilanyloxy)-4-methyldeca-4,6-dienyl]thiophene
Synonyms: 2-[(1RS,4E,6E)-10-(tert-butyldimethylsilanyloxy)-1-(tert-butyldiphenylsilanyloxy)-4-methyldeca-4,6-dienyl]thiophene
CAS NO:431990-36-2
Molecular Formula:
Molecular Weight: 619.072
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: 2-[(1RS,4E,6E)-10-(tert-butyldimethylsilanyloxy)-1-(tert-butyldiphenylsilanyloxy)-4-methyldeca-4,6-dienyl]thiophene(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(1RS,4E,6E)-10-(tert-butyldimethylsilanyloxy)-1-(tert-butyldiphenylsilanyloxy)-4-methyldeca-4,6-dienyl]thiophene(431990-36-2)
EPA Substance Registry System: 2-[(1RS,4E,6E)-10-(tert-butyldimethylsilanyloxy)-1-(tert-butyldiphenylsilanyloxy)-4-methyldeca-4,6-dienyl]thiophene(431990-36-2)

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: 431990-36-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 431990-36-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,1,9,9 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 431990-36:
(8*4)+(7*3)+(6*1)+(5*9)+(4*9)+(3*0)+(2*3)+(1*6)=152
152 % 10 = 2
So 431990-36-2 is a valid CAS Registry Number.

431990-36-2Upstream product

431990-36-2Downstream Products

431981-73-6 (4E,6E,10RS)-10-(tert-butyldiphenylsilanyloxy)-7-methyl-10-thiophen-2-yldeca-4,6-dien-1-ol

431990-36-2Relevant academic research and scientific papers

Synthesis and biological evaluation of structurally highly modified analogues of the antimitotic natural product curacin A

Wipf, Peter,Reeves, Jonathan T.,Balachandran, Raghavan,Day, Billy W.

, p. 1901 - 1917 (2007/10/03)

Structure-activity relationship analysis of synthetic analogues of curacin A revealed the lack of activity of traditional heterocyclic replacements of the thiazoline ring or cyclopropyl analogues of the core diene segment. The significance of the C(3)-C(4

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