Cas 515816-15-6,((4aR,5R,7R,8aS)-7-Benzyloxymethyl-2,2,4a-trimethyl-hexahydro-1,6-dioxa-2-sila-naphthalen-5-yl)-acetic acid ethyl ester

515816-15-6

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Basic information

Product Name: ((4aR,5R,7R,8aS)-7-Benzyloxymethyl-2,2,4a-trimethyl-hexahydro-1,6-dioxa-2-sila-naphthalen-5-yl)-acetic acid ethyl ester
Synonyms: ((4aR,5R,7R,8aS)-7-Benzyloxymethyl-2,2,4a-trimethyl-hexahydro-1,6-dioxa-2-sila-naphthalen-5-yl)-acetic acid ethyl ester
CAS NO:515816-15-6
Molecular Formula:
Molecular Weight: 406.594
EINECS: N/A
Product Categories: N/A
Mol File: 515816-15-6.mol
Article Data: 2

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: ((4aR,5R,7R,8aS)-7-Benzyloxymethyl-2,2,4a-trimethyl-hexahydro-1,6-dioxa-2-sila-naphthalen-5-yl)-acetic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: ((4aR,5R,7R,8aS)-7-Benzyloxymethyl-2,2,4a-trimethyl-hexahydro-1,6-dioxa-2-sila-naphthalen-5-yl)-acetic acid ethyl ester(515816-15-6)
EPA Substance Registry System: ((4aR,5R,7R,8aS)-7-Benzyloxymethyl-2,2,4a-trimethyl-hexahydro-1,6-dioxa-2-sila-naphthalen-5-yl)-acetic acid ethyl ester(515816-15-6)

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: 515816-15-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 515816-15-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,5,8,1 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 515816-15:
(8*5)+(7*1)+(6*5)+(5*8)+(4*1)+(3*6)+(2*1)+(1*5)=146
146 % 10 = 6
So 515816-15-6 is a valid CAS Registry Number.

515816-15-6Upstream product

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515816-15-6Relevant articles and documents

Lasonolide A: Structural revision and total synthesis

Song, Ho Young,Joo, Jung Min,Kang, Jung Won,Kim, Dae-Shik,Jung, Cheol-Kyu,Kwak, Hyo Shin,Park, Jin Hyun,Lee, Eun,Hong, Chang Yong,Jeong, ShinWu,Jeon, Kiwan

, p. 8080 - 8087 (2007/10/03)

The proposed structure of lasonolide A was synthesized employing radical cyclization reactions of β-alkoxyacrylates for preparation of the tetrahydropyranyl units A and B, but the spectroscopic data did not match those of the natural product. Both enantio

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