Cas 517920-45-5,2-Thiazolidinethione, 3-[(3R,4R)-4-cyclohexyl-3,4-dihydro-3-methyl-2-azetyl]-4-(1-methylethyl) -, (4S)-

517920-45-5

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Basic information

Product Name: 2-Thiazolidinethione, 3-[(3R,4R)-4-cyclohexyl-3,4-dihydro-3-methyl-2-azetyl]-4-(1-methylethyl) -, (4S)-
Synonyms:
CAS NO:517920-45-5
Molecular Formula: C16H26N2S2
Molecular Weight: 310.528
EINECS: N/A
Product Categories: N/A
Mol File: 517920-45-5.mol
Article Data: 2

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: 2-Thiazolidinethione, 3-[(3R,4R)-4-cyclohexyl-3,4-dihydro-3-methyl-2-azetyl]-4-(1-methylethyl) -, (4S)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Thiazolidinethione, 3-[(3R,4R)-4-cyclohexyl-3,4-dihydro-3-methyl-2-azetyl]-4-(1-methylethyl) -, (4S)-(517920-45-5)
EPA Substance Registry System: 2-Thiazolidinethione, 3-[(3R,4R)-4-cyclohexyl-3,4-dihydro-3-methyl-2-azetyl]-4-(1-methylethyl) -, (4S)-(517920-45-5)

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: 517920-45-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 517920-45-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,7,9,2 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 517920-45:
(8*5)+(7*1)+(6*7)+(5*9)+(4*2)+(3*0)+(2*4)+(1*5)=155
155 % 10 = 5
So 517920-45-5 is a valid CAS Registry Number.

517920-45-5Upstream product

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517920-45-5Relevant articles and documents

Diastereoselective addition of chlorotitanium enolate of N-acyl thiazolidinethione to O-methyl oximes: A novel, stereoselective synthesis of α,β-disubstituted β-amino carbonyl compounds via chiral auxiliary mediated azetine formation

Ambhaikar, Narendra B.,Snyder, James P.,Liotta, Dennis C.

, p. 3690 - 3691 (2003)

We have discovered a novel and highly diastereoselective synthesis of azetinyl thiazolidine-2-thiones that utilizes additions of the chlorotitanium enolates of N-acyl thiazolidin-2-thiones to O-methyl aldoximes. The "anti" azetines can be subsequently con

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