Cas 213330-41-7,(4S,5R)-4-((R)-2-Benzyloxy-1-methoxymethoxy-ethyl)-5-((E)-3-benzyloxy-propenyl)-[1,3]dioxolan-2-one

213330-41-7

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Basic information

Product Name: (4S,5R)-4-((R)-2-Benzyloxy-1-methoxymethoxy-ethyl)-5-((E)-3-benzyloxy-propenyl)-[1,3]dioxolan-2-one
Synonyms: (4S,5R)-4-((R)-2-Benzyloxy-1-methoxymethoxy-ethyl)-5-((E)-3-benzyloxy-propenyl)-[1,3]dioxolan-2-one
CAS NO:213330-41-7
Molecular Formula:
Molecular Weight: 428.482
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: (4S,5R)-4-((R)-2-Benzyloxy-1-methoxymethoxy-ethyl)-5-((E)-3-benzyloxy-propenyl)-[1,3]dioxolan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5R)-4-((R)-2-Benzyloxy-1-methoxymethoxy-ethyl)-5-((E)-3-benzyloxy-propenyl)-[1,3]dioxolan-2-one(213330-41-7)
EPA Substance Registry System: (4S,5R)-4-((R)-2-Benzyloxy-1-methoxymethoxy-ethyl)-5-((E)-3-benzyloxy-propenyl)-[1,3]dioxolan-2-one(213330-41-7)

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: 213330-41-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 213330-41-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,3,3 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 213330-41:
(8*2)+(7*1)+(6*3)+(5*3)+(4*3)+(3*0)+(2*4)+(1*1)=77
77 % 10 = 7
So 213330-41-7 is a valid CAS Registry Number.

213330-41-7Upstream product

213330-41-7Downstream Products

213330-41-7Relevant academic research and scientific papers

Concise enantioselective synthesis of (+)-aspicilin based on a ruthenium catalyzed olefin metathesis reaction

Nishioka, Toshiko,Iwabuchi, Yoshiharu,Irie, Hiroshi,Hatakeyama, Susumi

, p. 5597 - 5600 (1998)

An efficient enantioselective synthesis of (+)-aspicilin has been achieved in 12 steps from (2E,5E)-1,7-dibenzyloxy-2,5-heptadiene-4-ol employing Red-Al-promoted reductive cleavage of the benzyl 4-hydroxy-2- butenyl ether structure and ruthenium catalyzed

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