Cas 183556-46-9,Acrylic acid (3R,3aR,6S,6aR)-6-benzyloxy-hexahydro-furo[3,2-b]furan-3-yl ester

183556-46-9

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Basic information

Product Name: Acrylic acid (3R,3aR,6S,6aR)-6-benzyloxy-hexahydro-furo[3,2-b]furan-3-yl ester
Synonyms: Acrylic acid (3R,3aR,6S,6aR)-6-benzyloxy-hexahydro-furo[3,2-b]furan-3-yl ester
CAS NO:183556-46-9
Molecular Formula:
Molecular Weight: 290.316
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: Acrylic acid (3R,3aR,6S,6aR)-6-benzyloxy-hexahydro-furo[3,2-b]furan-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acrylic acid (3R,3aR,6S,6aR)-6-benzyloxy-hexahydro-furo[3,2-b]furan-3-yl ester(183556-46-9)
EPA Substance Registry System: Acrylic acid (3R,3aR,6S,6aR)-6-benzyloxy-hexahydro-furo[3,2-b]furan-3-yl ester(183556-46-9)

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: 183556-46-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 183556-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,5,5 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 183556-46:
(8*1)+(7*8)+(6*3)+(5*5)+(4*5)+(3*6)+(2*4)+(1*6)=159
159 % 10 = 9
So 183556-46-9 is a valid CAS Registry Number.

183556-46-9Upstream product

183556-46-9Downstream Products

183556-46-9Relevant academic research and scientific papers

Asymmetric Diels-Alder: Monobenzylated isosorbide and isomannide as highly effective chiral auxiliaries

Loupy, Andre,Monteux, Daphne

, p. 7023 - 7026 (1996)

Lewis acid promoted Diels-Alder reactions of acrylate esters from monobenzylated isosorbide or isomannide and cyclopentadiene provided exclusively endo-adducts with good yields and high diastereoselectivities. The R/S selectivities are quasi total and opposed using either isosorbide or isomannide derivatives.

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