Cas 128911-26-2,4-O-acetyl-1,2'-anhydro-3-C-ally-2,3-dideoxy-2-C-(2'-hydroxyethyl)-6-O-triphenylmethyl-α-D-glucopyranose

128911-26-2

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Basic information

Product Name: 4-O-acetyl-1,2'-anhydro-3-C-ally-2,3-dideoxy-2-C-(2'-hydroxyethyl)-6-O-triphenylmethyl-α-D-glucopyranose
Synonyms:
CAS NO:128911-26-2
Molecular Formula:
Molecular Weight: 498.619
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: 4-O-acetyl-1,2'-anhydro-3-C-ally-2,3-dideoxy-2-C-(2'-hydroxyethyl)-6-O-triphenylmethyl-α-D-glucopyranose(CAS DataBase Reference)
NIST Chemistry Reference: 4-O-acetyl-1,2'-anhydro-3-C-ally-2,3-dideoxy-2-C-(2'-hydroxyethyl)-6-O-triphenylmethyl-α-D-glucopyranose(128911-26-2)
EPA Substance Registry System: 4-O-acetyl-1,2'-anhydro-3-C-ally-2,3-dideoxy-2-C-(2'-hydroxyethyl)-6-O-triphenylmethyl-α-D-glucopyranose(128911-26-2)

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: 128911-26-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 128911-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,9,1 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 128911-26:
(8*1)+(7*2)+(6*8)+(5*9)+(4*1)+(3*1)+(2*2)+(1*6)=132
132 % 10 = 2
So 128911-26-2 is a valid CAS Registry Number.

128911-26-2Upstream product

126113-89-1 4,6-di-O-acetyl-1,2'-anhydro-3-C-ally-2,3-dideoxy-2-C-(2'-hydroxyethyl)-α-D-glucopyranose

128911-26-2Downstream Products

128911-26-2Relevant academic research and scientific papers

UNSATURATED CARBOHYDRATES. PART 29 THEIR APPLICATION TO THE SYNTHESIS OF STEREOSPECIFICALLY DOUBLY AND TRIPLY BRANCHED DERIVATIVES

Ferrier, Robert J.,Petersen, Paul M.

, p. 1 - 12 (1990)

Treatment of 2,3-dideoxy-α-D-erythro-hex-2-enopyranosyl derivatives having 2-haloethyl substituents separately at O-1 and O-4 with tri-n-butyltin hydride together with a radical initiator gave products 16 and 5,6 with tetrahydrofuranyl rings cis-fused to

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