Cas 1262326-52-2,allyl 4,5,7-tri-O-benzyl-2-bromo-2,3-dideoxy-α-D-arabino-hept-2-enoseptanoside

1262326-52-2

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Basic information

Product Name: allyl 4,5,7-tri-O-benzyl-2-bromo-2,3-dideoxy-α-D-arabino-hept-2-enoseptanoside
Synonyms:
CAS NO:1262326-52-2
Molecular Formula:
Molecular Weight: 565.504
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: allyl 4,5,7-tri-O-benzyl-2-bromo-2,3-dideoxy-α-D-arabino-hept-2-enoseptanoside(CAS DataBase Reference)
NIST Chemistry Reference: allyl 4,5,7-tri-O-benzyl-2-bromo-2,3-dideoxy-α-D-arabino-hept-2-enoseptanoside(1262326-52-2)
EPA Substance Registry System: allyl 4,5,7-tri-O-benzyl-2-bromo-2,3-dideoxy-α-D-arabino-hept-2-enoseptanoside(1262326-52-2)

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: 1262326-52-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1262326-52-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,3,2 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1262326-52:
(9*1)+(8*2)+(7*6)+(6*2)+(5*3)+(4*2)+(3*6)+(2*5)+(1*2)=132
132 % 10 = 2
So 1262326-52-2 is a valid CAS Registry Number.

1262326-52-2Upstream product

107-18-6 allyl alcohol

1262326-52-2Downstream Products

1262326-52-2Relevant academic research and scientific papers

Synthesis of C-furanosides from a d-glucal-derived cyclopropane through a ring-expansion/ring-contraction sequence

Hewitt, Russell J.,Harvey, Joanne E.

, p. 421 - 423 (2011)

gem-Dibromocyclopropane 1, prepared from tri-O-benzyl-d-glucal, undergoes thermal and silver-promoted ring expansion in the presence of alcohols to give substituted oxepines. With further heating, ring contraction to highly substituted tetrahydrofurans fo

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