Cas 344341-20-4,1-benzyloxy[2,2-dimethyl-(4S)-1,3-dioxolan-4-yl]methyl-(1R)-2-propenyl alcohol

344341-20-4

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Basic information

Product Name: 1-benzyloxy[2,2-dimethyl-(4S)-1,3-dioxolan-4-yl]methyl-(1R)-2-propenyl alcohol
Synonyms: 1-benzyloxy[2,2-dimethyl-(4S)-1,3-dioxolan-4-yl]methyl-(1R)-2-propenyl alcohol
CAS NO:344341-20-4
Molecular Formula:
Molecular Weight: 278.348
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-benzyloxy[2,2-dimethyl-(4S)-1,3-dioxolan-4-yl]methyl-(1R)-2-propenyl alcohol(CAS DataBase Reference)
NIST Chemistry Reference: 1-benzyloxy[2,2-dimethyl-(4S)-1,3-dioxolan-4-yl]methyl-(1R)-2-propenyl alcohol(344341-20-4)
EPA Substance Registry System: 1-benzyloxy[2,2-dimethyl-(4S)-1,3-dioxolan-4-yl]methyl-(1R)-2-propenyl alcohol(344341-20-4)

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: 344341-20-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 344341-20-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,4,3,4 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 344341-20:
(8*3)+(7*4)+(6*4)+(5*3)+(4*4)+(3*1)+(2*2)+(1*0)=114
114 % 10 = 4
So 344341-20-4 is a valid CAS Registry Number.

344341-20-4Upstream product

19877-13-5 3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-α-D-xylo-hex-5-enofuranose

344341-20-4Downstream Products

344341-21-5 3,4-dibenzyloxy-4-[2,2-dimethyl-(4S)-1,3-dioxolan-4-yl]-(3R)-1-butene

344341-20-4Relevant academic research and scientific papers

Pd(II)-mediated synthesis of 2-deoxy- and rare-C-glycosides

Sharma,Chander,Krishna, Palakodety Radha

, p. 539 - 544 (2001)

The synthesis of 2-deoxy-C-glycosides and rare-C-saccharides from the γ,δ-olefinic alcohols is described. In the presence of Pd(II) reagents these olefinic alcohols undergo an efficient intramolecular oxidative cyclisation to afford the target molecules.

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