Cas 1134474-75-1,(1S,2S,3R,6R)-3-benzyloxy-2-hydroxy-4,8,8-trimethyl-7,9-dioxadicyclo[4.3.0]non-4-ene

1134474-75-1

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Basic information

Product Name: (1S,2S,3R,6R)-3-benzyloxy-2-hydroxy-4,8,8-trimethyl-7,9-dioxadicyclo[4.3.0]non-4-ene
Synonyms: (1S,2S,3R,6R)-3-benzyloxy-2-hydroxy-4,8,8-trimethyl-7,9-dioxadicyclo[4.3.0]non-4-ene
CAS NO:1134474-75-1
Molecular Formula:
Molecular Weight: 304.343
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: (1S,2S,3R,6R)-3-benzyloxy-2-hydroxy-4,8,8-trimethyl-7,9-dioxadicyclo[4.3.0]non-4-ene(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S,3R,6R)-3-benzyloxy-2-hydroxy-4,8,8-trimethyl-7,9-dioxadicyclo[4.3.0]non-4-ene(1134474-75-1)
EPA Substance Registry System: (1S,2S,3R,6R)-3-benzyloxy-2-hydroxy-4,8,8-trimethyl-7,9-dioxadicyclo[4.3.0]non-4-ene(1134474-75-1)

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: 1134474-75-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1134474-75-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,4,4,7 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1134474-75:
(9*1)+(8*1)+(7*3)+(6*4)+(5*4)+(4*7)+(3*4)+(2*7)+(1*5)=141
141 % 10 = 1
So 1134474-75-1 is a valid CAS Registry Number.

1134474-75-1Upstream product

1134474-70-6 3-benzoyl-1,2,7,8-tetradeoxy-5,6-O-isopropylidene-2-C-methyl-D-altro-octa-1,7-dienitol

1134474-75-1Downstream Products

1134474-75-1Relevant academic research and scientific papers

Synthesis of gabosine A and N from ribose by the use of ring-closing metathesis

Monrad, Rune Nygaard,Fanefjord, Mette,Hansen, Flemming Gundorph,Jensen, N. Michael E.,Madsen, Robert

experimental part, p. 396 - 402 (2009/07/25)

A concise synthetic route is described for the synthesis of gabosine A and N. The key step uses a zinc-mediated tandem reaction where methyl 5-deoxy-5-iodo-2,3-O-isopropylidene-β-D-ribofuranoside is fragmented to give an unsaturated aldehyde which is ally

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