Cas 370858-92-7,(2R,3S,6RS)-4-methylbenzenesulfonic acid 6-[pent-4-enyloxy]-3-methyl-2-hydroxyhept-4-ynyl ester

370858-92-7

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Basic information

Product Name: (2R,3S,6RS)-4-methylbenzenesulfonic acid 6-[pent-4-enyloxy]-3-methyl-2-hydroxyhept-4-ynyl ester
Synonyms: (2R,3S,6RS)-4-methylbenzenesulfonic acid 6-[pent-4-enyloxy]-3-methyl-2-hydroxyhept-4-ynyl ester
CAS NO:370858-92-7
Molecular Formula:
Molecular Weight: 380.505
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: (2R,3S,6RS)-4-methylbenzenesulfonic acid 6-[pent-4-enyloxy]-3-methyl-2-hydroxyhept-4-ynyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S,6RS)-4-methylbenzenesulfonic acid 6-[pent-4-enyloxy]-3-methyl-2-hydroxyhept-4-ynyl ester(370858-92-7)
EPA Substance Registry System: (2R,3S,6RS)-4-methylbenzenesulfonic acid 6-[pent-4-enyloxy]-3-methyl-2-hydroxyhept-4-ynyl ester(370858-92-7)

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: 370858-92-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 370858-92-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,0,8,5 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 370858-92:
(8*3)+(7*7)+(6*0)+(5*8)+(4*5)+(3*8)+(2*9)+(1*2)=177
177 % 10 = 7
So 370858-92-7 is a valid CAS Registry Number.

370858-92-7Upstream product

370858-92-7Downstream Products

370858-92-7Relevant academic research and scientific papers

Stereoselective allylic transposition by means of allylic n-pentenyl ethers. Part 2: Synthesis of nitrogen heterocycles

Chouteau, Franck,Addi, Khadija,Bénéchie, Michel,Prangé, Thierry,Khuong-Huu, Fran?oise

, p. 6229 - 6238 (2001)

Stereospecific synthesis of optically active substituted pyrrolidines, and piperidines was studied via an intramolecular allylic rearrangement by means of allylic n-pentenyl ethers as leaving groups when reacting with halonium ions.

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