Cas 903504-03-0,(3-benzyl-5-phenyl-2-trifluoromethyl-pent-2-en-4-ynyloxy)-<i>tert</i>-butyl-dimethyl-silane

903504-03-0

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Basic information

Product Name: (3-benzyl-5-phenyl-2-trifluoromethyl-pent-2-en-4-ynyloxy)-tert-butyl-dimethyl-silane
Synonyms: (3-benzyl-5-phenyl-2-trifluoromethyl-pent-2-en-4-ynyloxy)-tert-butyl-dimethyl-silane
CAS NO:903504-03-0
Molecular Formula:
Molecular Weight: 430.585
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: (3-benzyl-5-phenyl-2-trifluoromethyl-pent-2-en-4-ynyloxy)-tert-butyl-dimethyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: (3-benzyl-5-phenyl-2-trifluoromethyl-pent-2-en-4-ynyloxy)-tert-butyl-dimethyl-silane(903504-03-0)
EPA Substance Registry System: (3-benzyl-5-phenyl-2-trifluoromethyl-pent-2-en-4-ynyloxy)-tert-butyl-dimethyl-silane(903504-03-0)

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: 903504-03-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 903504-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,3,5,0 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 903504-03:
(8*9)+(7*0)+(6*3)+(5*5)+(4*0)+(3*4)+(2*0)+(1*3)=130
130 % 10 = 0
So 903504-03-0 is a valid CAS Registry Number.

903504-03-0Upstream product

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903504-03-0Relevant academic research and scientific papers

Highly efficient synthesis of 4-trifluoromethylfuran derivatives via a sequential deprotection-annulation reaction

Zhang, Jiming,Zhao, Xiaoming,Li, Youhua,Lu, Long

, p. 4737 - 4739 (2007/10/03)

(E)-O-protected-2-trifluoromethyl-1-bromo-1-substituted allylic alcohol reacted with terminal alkynes under Sonogashira reaction condition to give the corresponding (E)-2-en-4-ynoic alcohol derivatives, which was further converted to the corresponding 4-t

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