Cas 946416-39-3,1,5-anhydro-2,3,4,6-tetra-O-benzyl-1,2-C-(dichloromethylene)-α-D-glycero-L-altro-hexitol

946416-39-3

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Basic information

Product Name: 1,5-anhydro-2,3,4,6-tetra-O-benzyl-1,2-C-(dichloromethylene)-α-D-glycero-L-altro-hexitol
Synonyms: 1,5-anhydro-2,3,4,6-tetra-O-benzyl-1,2-C-(dichloromethylene)-α-D-glycero-L-altro-hexitol
CAS NO:946416-39-3
Molecular Formula:
Molecular Weight: 605.558
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: 1,5-anhydro-2,3,4,6-tetra-O-benzyl-1,2-C-(dichloromethylene)-α-D-glycero-L-altro-hexitol(CAS DataBase Reference)
NIST Chemistry Reference: 1,5-anhydro-2,3,4,6-tetra-O-benzyl-1,2-C-(dichloromethylene)-α-D-glycero-L-altro-hexitol(946416-39-3)
EPA Substance Registry System: 1,5-anhydro-2,3,4,6-tetra-O-benzyl-1,2-C-(dichloromethylene)-α-D-glycero-L-altro-hexitol(946416-39-3)

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: 946416-39-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 946416-39-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,6,4,1 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 946416-39:
(8*9)+(7*4)+(6*6)+(5*4)+(4*1)+(3*6)+(2*3)+(1*9)=193
193 % 10 = 3
So 946416-39-3 is a valid CAS Registry Number.

946416-39-3Upstream product

946416-39-3Downstream Products

946416-39-3Relevant academic research and scientific papers

Synthesis of septanosides through an oxyglycal route

Vijaya Ganesh,Jayaraman

, p. 5500 - 5504 (2007)

(Chemical Equation Presented) A new route to synthesize septanoside derivatives from protected 2-hydroxyglycals is reported. Ring expansion of a pyranoside to a septanoside was achieved through key reactions of a cyclopropanation, ring opening, oxidation,

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