Cas 144686-22-6,4-Thiazolidinecarboxamide, N-cyclohexyl-3-[3-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxopropyl]- 2,2,5,5-tetramethyl-

144686-22-6

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Basic information

Product Name: 4-Thiazolidinecarboxamide, N-cyclohexyl-3-[3-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxopropyl]- 2,2,5,5-tetramethyl-
Synonyms:
CAS NO:144686-22-6
Molecular Formula: C25H33N3O4S
Molecular Weight: 471.621
EINECS: N/A
Product Categories: N/A
Mol File: 144686-22-6.mol

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: 4-Thiazolidinecarboxamide, N-cyclohexyl-3-[3-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxopropyl]- 2,2,5,5-tetramethyl-(CAS DataBase Reference)
NIST Chemistry Reference: 4-Thiazolidinecarboxamide, N-cyclohexyl-3-[3-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxopropyl]- 2,2,5,5-tetramethyl-(144686-22-6)
EPA Substance Registry System: 4-Thiazolidinecarboxamide, N-cyclohexyl-3-[3-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxopropyl]- 2,2,5,5-tetramethyl-(144686-22-6)

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: 144686-22-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 144686-22-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,6,8 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 144686-22:
(8*1)+(7*4)+(6*4)+(5*6)+(4*8)+(3*6)+(2*2)+(1*2)=146
146 % 10 = 6
So 144686-22-6 is a valid CAS Registry Number.

144686-22-6Upstream product

144686-22-6Downstream Products

144686-17-9 3-(3-Amino-propionyl)-2,2,5,5-tetramethyl-thiazolidine-4-carboxylic acid cyclohexylamide

144686-22-6Relevant academic research and scientific papers

Simplified synthesis of peptides with non-protected amino acid hydrochlorides via four-component condensation

Kintscher,Martens

, p. 837 - 838 (1992)

Synthesis of sulfur containing peptide analogues, 3-(ω-aminoalkanoyl)-2,2-dimethyl-1,3-thiazolidine-4-carboxamides 2, via Ugi four-component condensation (4CC) starting from 2,5-dihydro-1,3-thiazoles 1, isocyanides and non-protected amino acid hydrochlori

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