Cas 609769-08-6,Acetic acid (1R,5R,6S)-3-((3R,4S,6R)-6-acetoxy-4-benzyloxymethoxy-3-chloro-cyclohept-1-enylmethyl)-6-benzyloxymethoxy-5-chloro-cyclohept-3-enyl ester

609769-08-6

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Basic information

Product Name: Acetic acid (1R,5R,6S)-3-((3R,4S,6R)-6-acetoxy-4-benzyloxymethoxy-3-chloro-cyclohept-1-enylmethyl)-6-benzyloxymethoxy-5-chloro-cyclohept-3-enyl ester
Synonyms: Acetic acid (1R,5R,6S)-3-((3R,4S,6R)-6-acetoxy-4-benzyloxymethoxy-3-chloro-cyclohept-1-enylmethyl)-6-benzyloxymethoxy-5-chloro-cyclohept-3-enyl ester
CAS NO:609769-08-6
Molecular Formula:
Molecular Weight: 661.62
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 (1R,5R,6S)-3-((3R,4S,6R)-6-acetoxy-4-benzyloxymethoxy-3-chloro-cyclohept-1-enylmethyl)-6-benzyloxymethoxy-5-chloro-cyclohept-3-enyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (1R,5R,6S)-3-((3R,4S,6R)-6-acetoxy-4-benzyloxymethoxy-3-chloro-cyclohept-1-enylmethyl)-6-benzyloxymethoxy-5-chloro-cyclohept-3-enyl ester(609769-08-6)
EPA Substance Registry System: Acetic acid (1R,5R,6S)-3-((3R,4S,6R)-6-acetoxy-4-benzyloxymethoxy-3-chloro-cyclohept-1-enylmethyl)-6-benzyloxymethoxy-5-chloro-cyclohept-3-enyl ester(609769-08-6)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 609769-08-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 609769-08-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,9,7,6 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 609769-08:
(8*6)+(7*0)+(6*9)+(5*7)+(4*6)+(3*9)+(2*0)+(1*8)=196
196 % 10 = 6
So 609769-08-6 is a valid CAS Registry Number.

609769-08-6Upstream product

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609769-08-6Relevant academic research and scientific papers

An expeditious, non-iterative, and asymmetric synthesis of 3,5,7,9,11,13,15-heptahydroxypentadecanals

Gerber-Lemaire, Sandrine,Vogel, Pierre

, p. 2959 - 2963 (2003)

Ozonolysis of (1R,1′R,6R,6′R)-3,3′-methylenebis{6-[(benzyloxy) methoxy]cyclohept-3-en-1-ol} followed by the diastereoselective reduction of the resulting β-hydroxy ketone intermediates gives a rapid route to long-chain polyketides bearing unsymmetrical functions at their terminal positions. These can easily be converted into enantiomerically pure long-chain 1,3-polyol fragments. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

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