Cas 1049006-95-2,methyl 2,3,4,9,10,11-hexa-O-benzyl-7,8-dideoxy-7,8-didehydro-12,13-O-isopropylidene-α-D-gluco-D-gluco-tridec-7(E)-eno-1,5-pyranosid-6-ulose

1049006-95-2

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Basic information

Product Name: methyl 2,3,4,9,10,11-hexa-O-benzyl-7,8-dideoxy-7,8-didehydro-12,13-O-isopropylidene-α-D-gluco-D-gluco-tridec-7(E)-eno-1,5-pyranosid-6-ulose
Synonyms: methyl 2,3,4,9,10,11-hexa-O-benzyl-7,8-dideoxy-7,8-didehydro-12,13-O-isopropylidene-α-D-gluco-D-gluco-tridec-7(E)-eno-1,5-pyranosid-6-ulose
CAS NO:1049006-95-2
Molecular Formula:
Molecular Weight: 949.151
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: methyl 2,3,4,9,10,11-hexa-O-benzyl-7,8-dideoxy-7,8-didehydro-12,13-O-isopropylidene-α-D-gluco-D-gluco-tridec-7(E)-eno-1,5-pyranosid-6-ulose(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2,3,4,9,10,11-hexa-O-benzyl-7,8-dideoxy-7,8-didehydro-12,13-O-isopropylidene-α-D-gluco-D-gluco-tridec-7(E)-eno-1,5-pyranosid-6-ulose(1049006-95-2)
EPA Substance Registry System: methyl 2,3,4,9,10,11-hexa-O-benzyl-7,8-dideoxy-7,8-didehydro-12,13-O-isopropylidene-α-D-gluco-D-gluco-tridec-7(E)-eno-1,5-pyranosid-6-ulose(1049006-95-2)

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: 1049006-95-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1049006-95-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,9,0,0 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1049006-95:
(9*1)+(8*0)+(7*4)+(6*9)+(5*0)+(4*0)+(3*6)+(2*9)+(1*5)=132
132 % 10 = 2
So 1049006-95-2 is a valid CAS Registry Number.

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1049006-95-2Relevant academic research and scientific papers

Synthesis of higher carbon sugars. Unexpected rearrangement of higher sugar allylic alcohols

Jarosz, Slawomir,Gajewska, Agnieszka,Luboradzki, Roman

, p. 1385 - 1391 (2008/12/20)

Coupling of a sugar phosphonate with a sugar aldehyde afforded a C13-higher sugar enone. Reduction of the carbonyl function provided both stereoisomeric allylic alcohols. Inversion of the configuration at the carbinol centre in these derivatives did not yield the expected SN2 product, but proceeded with rearrangement to the tetrahydrofuran derivative.

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