Cas 102794-52-5,Carbonic acid allyl ester (2S,3S,4R)-2,3,5-tris-benzyloxy-4-[((E)-propenyl)oxy]-pentyl ester

102794-52-5

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Basic information

Product Name: Carbonic acid allyl ester (2S,3S,4R)-2,3,5-tris-benzyloxy-4-[((E)-propenyl)oxy]-pentyl ester
Synonyms:
CAS NO:102794-52-5
Molecular Formula:
Molecular Weight: 546.661
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: Carbonic acid allyl ester (2S,3S,4R)-2,3,5-tris-benzyloxy-4-[((E)-propenyl)oxy]-pentyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbonic acid allyl ester (2S,3S,4R)-2,3,5-tris-benzyloxy-4-[((E)-propenyl)oxy]-pentyl ester(102794-52-5)
EPA Substance Registry System: Carbonic acid allyl ester (2S,3S,4R)-2,3,5-tris-benzyloxy-4-[((E)-propenyl)oxy]-pentyl ester(102794-52-5)

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: 102794-52-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 102794-52-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,7,9 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102794-52:
(8*1)+(7*0)+(6*2)+(5*7)+(4*9)+(3*4)+(2*5)+(1*2)=115
115 % 10 = 5
So 102794-52-5 is a valid CAS Registry Number.

102794-52-5Upstream product

102794-46-7 Carbonic acid allyl ester (2S,3R,4R)-4-allyloxy-2,3,5-tris-benzyloxy-pentyl ester

102794-52-5Downstream Products

102794-52-5Relevant academic research and scientific papers

THE RELATIVE STABILITY OF ALLYL ETHER, ALLYLOXYCARBONYL ESTER AND PROP-2 ENYLIDENE ACETAL, PROTECTIVE GROUPS TOWARD IRIDIUM, RHODIUM AND PALLADIUM CATALYSTS.

Kloosterman, M,Boom, J. H. Van,Chatelard, P.,Boullanger. P.,Descotes, G.

, p. 5045 - 5048 (2007/10/02)

The deprotection of allyloxycarbonyl derivatives of sugars was realized in the presence of allylether or prop-2-enylidene acetal with Pd(PPh3)4 or RhCl(PPh3)3 as catalyst while PF6 isomerized selectively the allyl ethers.

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