Cas 1239335-44-4,(E)-3,5-bis(benzyloxy)-2-(3',4'-bis(benzyloxy)phenyl)allylphenyltrifluoromethane sulfonate

1239335-44-4

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Basic information

Product Name: (E)-3,5-bis(benzyloxy)-2-(3',4'-bis(benzyloxy)phenyl)allylphenyltrifluoromethane sulfonate
Synonyms: (E)-3,5-bis(benzyloxy)-2-(3',4'-bis(benzyloxy)phenyl)allylphenyltrifluoromethane sulfonate
CAS NO:1239335-44-4
Molecular Formula:
Molecular Weight: 766.835
EINECS: N/A
Product Categories: N/A
Mol File: 1239335-44-4.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: (E)-3,5-bis(benzyloxy)-2-(3',4'-bis(benzyloxy)phenyl)allylphenyltrifluoromethane sulfonate(CAS DataBase Reference)
NIST Chemistry Reference: (E)-3,5-bis(benzyloxy)-2-(3',4'-bis(benzyloxy)phenyl)allylphenyltrifluoromethane sulfonate(1239335-44-4)
EPA Substance Registry System: (E)-3,5-bis(benzyloxy)-2-(3',4'-bis(benzyloxy)phenyl)allylphenyltrifluoromethane sulfonate(1239335-44-4)

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: 1239335-44-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1239335-44-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,9,3,3 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1239335-44:
(9*1)+(8*2)+(7*3)+(6*9)+(5*3)+(4*3)+(3*5)+(2*4)+(1*4)=154
154 % 10 = 4
So 1239335-44-4 is a valid CAS Registry Number.

1239335-44-4Upstream product

1239335-44-4Downstream Products

1239335-45-5 (E)-(3,5-bis(benzyloxy)-2-(3-(3',4'-bis(benzyloxy)phenyl)allyl)phenyl)tert-butylsulfane

1239335-44-4Relevant articles and documents

Enantioselctive syntheses of sulfur analogues of flavan-3-ols

Sharma, Pradeep K.,He, Min,Jurayj, Jurjus,Gou, Da-Ming,Lombardy, Richard,Romanczyk Jr., Leo J.,Schroeter, Hagen

experimental part, p. 5595 - 5619 (2010/12/18)

The first enantioselective syntheses of sulfur flavan-3-ol analogues 1-8 have been accomplished, whereby the oxygen atom of the pyran ring has been replaced by a sulfur atom. The key steps were: (a) Pd(0) catalyzed introduction of -S t-butyl group, (b) Sh

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