Cas 183073-34-9,(3aR,4R,6aR)-6a-Benzyloxymethyl-4-methoxy-3-methylene-hexahydro-furo[3,4-b]furan

183073-34-9

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Basic information

Product Name: (3aR,4R,6aR)-6a-Benzyloxymethyl-4-methoxy-3-methylene-hexahydro-furo[3,4-b]furan
Synonyms: (3aR,4R,6aR)-6a-Benzyloxymethyl-4-methoxy-3-methylene-hexahydro-furo[3,4-b]furan
CAS NO:183073-34-9
Molecular Formula:
Molecular Weight: 276.332
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: (3aR,4R,6aR)-6a-Benzyloxymethyl-4-methoxy-3-methylene-hexahydro-furo[3,4-b]furan(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,4R,6aR)-6a-Benzyloxymethyl-4-methoxy-3-methylene-hexahydro-furo[3,4-b]furan(183073-34-9)
EPA Substance Registry System: (3aR,4R,6aR)-6a-Benzyloxymethyl-4-methoxy-3-methylene-hexahydro-furo[3,4-b]furan(183073-34-9)

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: 183073-34-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 183073-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,0,7 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 183073-34:
(8*1)+(7*8)+(6*3)+(5*0)+(4*7)+(3*3)+(2*3)+(1*4)=129
129 % 10 = 9
So 183073-34-9 is a valid CAS Registry Number.

183073-34-9Upstream product

183073-34-9Downstream Products

183073-36-1 (3aR,4R,6aR)-6a-Benzyloxymethyl-4-methoxy-3-methylene-tetrahydro-furo[3,4-b]furan-2-one

183073-34-9Relevant academic research and scientific papers

Synthesis of Bis-γ-Butyrolactones Containing Conformationally Constrained (S)- and (R)-Diacylglycerol Structures

Lee, Jeewoo,Lewin, Nancy E.,Blumberg, Peter M.,Marquez, Victor E.

, p. 1299 - 1306 (1996)

The synthesis of two sets of rigid diacylglycerol (DAG) analogues with either the (S)-DAG or (R)-DAG enantiomer embedded into a bis-γ-butyrolactone template was accomplished stereoselectively from di-O-isopropylidene-α-D-apiose.The key step in both synthe

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