Cas 537698-04-7,1,3-Dithiane-2-octanoic acid, 2-[(1E,3S,4R)-4-(acetyloxy)-3-[[tris(1-methylethyl)silyl]oxy]-1-nonenyl]-, 1,1-dimethylethyl ester

537698-04-7

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Basic information

Product Name: 1,3-Dithiane-2-octanoic acid, 2-[(1E,3S,4R)-4-(acetyloxy)-3-[[tris(1-methylethyl)silyl]oxy]-1-nonenyl]-, 1,1-dimethylethyl ester
Synonyms:
CAS NO:537698-04-7
Molecular Formula: C36H68O5S2Si
Molecular Weight: 673.15
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: 1,3-Dithiane-2-octanoic acid, 2-[(1E,3S,4R)-4-(acetyloxy)-3-[[tris(1-methylethyl)silyl]oxy]-1-nonenyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1,3-Dithiane-2-octanoic acid, 2-[(1E,3S,4R)-4-(acetyloxy)-3-[[tris(1-methylethyl)silyl]oxy]-1-nonenyl]-, 1,1-dimethylethyl ester(537698-04-7)
EPA Substance Registry System: 1,3-Dithiane-2-octanoic acid, 2-[(1E,3S,4R)-4-(acetyloxy)-3-[[tris(1-methylethyl)silyl]oxy]-1-nonenyl]-, 1,1-dimethylethyl ester(537698-04-7)

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: 537698-04-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 537698-04-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,7,6,9 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 537698-04:
(8*5)+(7*3)+(6*7)+(5*6)+(4*9)+(3*8)+(2*0)+(1*4)=197
197 % 10 = 7
So 537698-04-7 is a valid CAS Registry Number.

537698-04-7Upstream product

80522-42-5 triisopropylsilyl trifluoromethanesulfonate

537698-04-7Downstream Products

537698-04-7Relevant academic research and scientific papers

Total synthesis and adjuvant activity of all stereoisomers of pinellic acid

Shirahata, Tatsuya,Sunazuka, Toshiaki,Yoshida, Kiminari,Yamamoto, Daisuke,Harigaya, Yoshihiko,Nagai, Takayuki,Kiyohara, Hiroaki,Yamada, Haruki,Kuwajima, Isao,Omura, Satoshi

, p. 937 - 941 (2003)

Pinellic acid is a novel and potentially useful oral adjuvant when used in conjunction with intranasal inoculation of influenza HA vaccines. All stereoisomers of pinellic acid have been synthesized via regioselective asymmetric dihydroxylation, regioselective inversion, and stereoselective reduction, and their adjuvant activities were characterized. Among this series of isomers, 9S, 12S, 13S compound has the most potent adjuvant activity. Structure-activity relationships are discussed.

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