Cas 24099-02-3,(4-formyl-5-methyl-2-phenyl-2<i>H</i>-pyrazol-3-ylsulfanyl)-acetic acid

24099-02-3

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Basic information

Product Name: (4-formyl-5-methyl-2-phenyl-2H-pyrazol-3-ylsulfanyl)-acetic acid
Synonyms: (4-formyl-5-methyl-2-phenyl-2H-pyrazol-3-ylsulfanyl)-acetic acid
CAS NO:24099-02-3
Molecular Formula:
Molecular Weight: 276.316
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: (4-formyl-5-methyl-2-phenyl-2H-pyrazol-3-ylsulfanyl)-acetic acid(CAS DataBase Reference)
NIST Chemistry Reference: (4-formyl-5-methyl-2-phenyl-2H-pyrazol-3-ylsulfanyl)-acetic acid(24099-02-3)
EPA Substance Registry System: (4-formyl-5-methyl-2-phenyl-2H-pyrazol-3-ylsulfanyl)-acetic acid(24099-02-3)

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: 24099-02-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 24099-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,9 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24099-02:
(7*2)+(6*4)+(5*0)+(4*9)+(3*9)+(2*0)+(1*2)=103
103 % 10 = 3
So 24099-02-3 is a valid CAS Registry Number.

24099-02-3Upstream product

24099-02-3Downstream Products

24099-02-3Relevant academic research and scientific papers

One-step assembly of carbamoyl-substituted heteroannelated [1,4]thiazepines

Ilyn, Alexey P.,Loseva, Marina V.,Vvedensky, Vladimir Y.,Putsykina, Elena B.,Tkachenko, Sergey E.,Kravchenko, Dmitri V.,Khvat, Alexandr V.,Krasavin, Mikhail Y.,Ivachtchenko, Alexandre V.

, p. 2811 - 2819 (2007/10/03)

We present a convenient synthesis of novel heteroaryl-fused 3-oxo-1,4-thiazepine-5-carboxamides and 5-oxo-1,4-thiazepine-3-carboxamides using a modification of four-component Ugi condensation. We demonstrate the usefulness and versatility of the developed approach for the synthesis of variously substituted compounds and discuss the scope and limitations of the chemistry involved.

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