Cas 79621-95-7,(4aR,6S,8aS)-8-[1-Butoxy-meth-(E)-ylidene]-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine

79621-95-7

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Basic information

Product Name: (4aR,6S,8aS)-8-[1-Butoxy-meth-(E)-ylidene]-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine
Synonyms: (4aR,6S,8aS)-8-[1-Butoxy-meth-(E)-ylidene]-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine
CAS NO:79621-95-7
Molecular Formula:
Molecular Weight: 334.412
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: (4aR,6S,8aS)-8-[1-Butoxy-meth-(E)-ylidene]-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine(CAS DataBase Reference)
NIST Chemistry Reference: (4aR,6S,8aS)-8-[1-Butoxy-meth-(E)-ylidene]-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine(79621-95-7)
EPA Substance Registry System: (4aR,6S,8aS)-8-[1-Butoxy-meth-(E)-ylidene]-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine(79621-95-7)

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: 79621-95-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 79621-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,2 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79621-95:
(7*7)+(6*9)+(5*6)+(4*2)+(3*1)+(2*9)+(1*5)=167
167 % 10 = 7
So 79621-95-7 is a valid CAS Registry Number.

79621-95-7Upstream product

79621-95-7Downstream Products

79607-56-0 Methyl 4,6-O-benzylidene-2-deoxy-3-C-formyl-α-D-arabino-hexopyranoside

79621-95-7Relevant academic research and scientific papers

SEHR EINFACHES SYNTHESEPRINZIP FUER FORMYL-VERZWEIGTE KOHLENHYDRATE VOM STREPTOSE-TYP

Dyong, Ingolf,Weigand, Joachim,Meyer, Wolfgang

, p. 2969 - 2970 (1981)

n-Butylvinyl ethers, prepared by Wittig olefination of aldos-3-ulose derivatives react upon osmium tetraoxide hydroxylation with immediate formation of OH-C-CHO branched carbohydrates.

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