Cas 792935-81-0,D-arabino-Hex-5-enitol, 1,6-anhydro-5-deoxy-3,4-O-(1-methylethylidene)-, acetate (9CI)

792935-81-0

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Basic information

Product Name: D-arabino-Hex-5-enitol, 1,6-anhydro-5-deoxy-3,4-O-(1-methylethylidene)-, acetate (9CI)
Synonyms: D-arabino-Hex-5-enitol, 1,6-anhydro-5-deoxy-3,4-O-(1-methylethylidene)-, acetate (9CI)
CAS NO:792935-81-0
Molecular Formula: C11H16O5
Molecular Weight: 228.24174
EINECS: N/A
Product Categories: METHYL
Mol File: 792935-81-0.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: D-arabino-Hex-5-enitol, 1,6-anhydro-5-deoxy-3,4-O-(1-methylethylidene)-, acetate (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: D-arabino-Hex-5-enitol, 1,6-anhydro-5-deoxy-3,4-O-(1-methylethylidene)-, acetate (9CI)(792935-81-0)
EPA Substance Registry System: D-arabino-Hex-5-enitol, 1,6-anhydro-5-deoxy-3,4-O-(1-methylethylidene)-, acetate (9CI)(792935-81-0)

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: 792935-81-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 792935-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,2,9,3 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 792935-81:
(8*7)+(7*9)+(6*2)+(5*9)+(4*3)+(3*5)+(2*8)+(1*1)=220
220 % 10 = 0
So 792935-81-0 is a valid CAS Registry Number.

792935-81-0Upstream product

792935-81-0Downstream Products

792935-81-0Relevant academic research and scientific papers

Synthesis of seven-membered ring glycals via endo-selective alkynol cycloisomerization

Alcázar, Eva,Pletcher, Joseph M.,McDonald, Frank E.

, p. 3877 - 3880 (2004)

Alkynyldiols 1 undergo cycloisomerization to the corresponding seven-membered cyclic enol ethers 2 under tungsten carbonyl catalysis. This novel transformation proceeds with good yields and virtually complete regioselectivity for all diastereomers of 1, f

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