Cas 175673-34-4,(E)-(4S,5S,6R)-7-Benzyloxy-5-hydroxy-2,4,6-trimethyl-hept-2-enoic acid ethyl ester

175673-34-4

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Basic information

Product Name: (E)-(4S,5S,6R)-7-Benzyloxy-5-hydroxy-2,4,6-trimethyl-hept-2-enoic acid ethyl ester
Synonyms: (E)-(4S,5S,6R)-7-Benzyloxy-5-hydroxy-2,4,6-trimethyl-hept-2-enoic acid ethyl ester
CAS NO:175673-34-4
Molecular Formula:
Molecular Weight: 320.429
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: (E)-(4S,5S,6R)-7-Benzyloxy-5-hydroxy-2,4,6-trimethyl-hept-2-enoic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-(4S,5S,6R)-7-Benzyloxy-5-hydroxy-2,4,6-trimethyl-hept-2-enoic acid ethyl ester(175673-34-4)
EPA Substance Registry System: (E)-(4S,5S,6R)-7-Benzyloxy-5-hydroxy-2,4,6-trimethyl-hept-2-enoic acid ethyl ester(175673-34-4)

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: 175673-34-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 175673-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,6,7 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 175673-34:
(8*1)+(7*7)+(6*5)+(5*6)+(4*7)+(3*3)+(2*3)+(1*4)=164
164 % 10 = 4
So 175673-34-4 is a valid CAS Registry Number.

175673-34-4Upstream product

75-24-1 trimethylaluminum

175673-34-4Downstream Products

175673-34-4Relevant academic research and scientific papers

A stereocontrolled enantiospecific route to tirandamycin B

Shiratani, Tomonori,Kimura, Kiyoshi,Yoshihara, Kousei,Hatakeyama, Susumi,Irie, Hiroshi,Miyashita, Masaaki

, p. 21 - 22 (1996)

The enal 15 was synthesized in enantiomerically pure form starting from (S)-3-benzyloxy-2-methylpropanol 3 via highly regio- and stereo-selective methylation of the γ,δ-epoxy acrylate 5 with trimethylaluminium in the presence of water, developing an enantiospecific route to tirandamycin B.

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