Cas 516457-82-2,Acetic acid (6Z,9Z)-(1S,5S,13S,15S)-10-chloro-15-(4-methoxy-benzyloxymethyl)-6-methyl-3-oxo-2,14-dioxa-bicyclo[11.2.1]hexadeca-6,9-dien-5-yl ester

516457-82-2

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Basic information

Product Name: Acetic acid (6Z,9Z)-(1S,5S,13S,15S)-10-chloro-15-(4-methoxy-benzyloxymethyl)-6-methyl-3-oxo-2,14-dioxa-bicyclo[11.2.1]hexadeca-6,9-dien-5-yl ester
Synonyms: Acetic acid (6Z,9Z)-(1S,5S,13S,15S)-10-chloro-15-(4-methoxy-benzyloxymethyl)-6-methyl-3-oxo-2,14-dioxa-bicyclo[11.2.1]hexadeca-6,9-dien-5-yl ester
CAS NO:516457-82-2
Molecular Formula:
Molecular Weight: 492.997
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: Acetic acid (6Z,9Z)-(1S,5S,13S,15S)-10-chloro-15-(4-methoxy-benzyloxymethyl)-6-methyl-3-oxo-2,14-dioxa-bicyclo[11.2.1]hexadeca-6,9-dien-5-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (6Z,9Z)-(1S,5S,13S,15S)-10-chloro-15-(4-methoxy-benzyloxymethyl)-6-methyl-3-oxo-2,14-dioxa-bicyclo[11.2.1]hexadeca-6,9-dien-5-yl ester(516457-82-2)
EPA Substance Registry System: Acetic acid (6Z,9Z)-(1S,5S,13S,15S)-10-chloro-15-(4-methoxy-benzyloxymethyl)-6-methyl-3-oxo-2,14-dioxa-bicyclo[11.2.1]hexadeca-6,9-dien-5-yl ester(516457-82-2)

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: 516457-82-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 516457-82-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,6,4,5 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 516457-82:
(8*5)+(7*1)+(6*6)+(5*4)+(4*5)+(3*7)+(2*8)+(1*2)=162
162 % 10 = 2
So 516457-82-2 is a valid CAS Registry Number.

516457-82-2Upstream product

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516457-82-2Relevant academic research and scientific papers

Enantioselective synthesis of 15-epi-haterumalide NA methyl ester and revised structure of haterumalide NA

Kigoshi, Hideo,Kita, Masaki,Ogawa, Seiji,Itoh, Masahiro,Uemura, Daisuke

, p. 957 - 960 (2003)

(Matrix presented). The enantioselective synthesis of the enantiomer of the haterumalide NA methyl ester, a cytotoxic macrolide from an Okinawan sponge, was achieved from the threitol derivative in 26 steps. The key steps are the stereoselective construct

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