Cas 1135538-97-4,4-(1-hydroxycyclohexyl)-1-(4-methylbenzenesulfonyl)-1,2,3-triazole

1135538-97-4

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Basic information

Product Name: 4-(1-hydroxycyclohexyl)-1-(4-methylbenzenesulfonyl)-1,2,3-triazole
Synonyms: 4-(1-hydroxycyclohexyl)-1-(4-methylbenzenesulfonyl)-1,2,3-triazole
CAS NO:1135538-97-4
Molecular Formula:
Molecular Weight: 321.4
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-(1-hydroxycyclohexyl)-1-(4-methylbenzenesulfonyl)-1,2,3-triazole(CAS DataBase Reference)
NIST Chemistry Reference: 4-(1-hydroxycyclohexyl)-1-(4-methylbenzenesulfonyl)-1,2,3-triazole(1135538-97-4)
EPA Substance Registry System: 4-(1-hydroxycyclohexyl)-1-(4-methylbenzenesulfonyl)-1,2,3-triazole(1135538-97-4)

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: 1135538-97-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1135538-97-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,5,5,3 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1135538-97:
(9*1)+(8*1)+(7*3)+(6*5)+(5*5)+(4*3)+(3*8)+(2*9)+(1*7)=154
154 % 10 = 4
So 1135538-97-4 is a valid CAS Registry Number.

1135538-97-4Upstream product

1135538-97-4Downstream Products

1135538-97-4Relevant academic research and scientific papers

METHOD OF PRODUCING SULFONYL OR SULFAMOYL TRIAZOLE-BASED COMPOUNDS USING CONTINUOUS FLOW PROCESS

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Paragraph 0099-0103, (2019/12/25)

The present invention relates to a method for manufacturing a sulfonyl or sulfamoyl triazole-based compound using a continuous flow process. According to embodiments of the present specification, the sulfonyl or sulfamoyl triazole-based compound frequentl

Ring expansion and rearrangements of rhodium(II) azavinyl carbenes

Selander, Nicklas,Worrell, Brady T.,Fokin, Valery V.

supporting information, p. 13054 - 13057 (2013/03/14)

The ring expansion and rearrangement of diazo compounds, specifically rhodium carbenes (derived from the corresponding diazo species), is an efficient and operationally simple method for the construction of structurally unique frameworks.[ 1] Products der

Synthesis of enaminones by rhodium-catalyzed denitrogenative rearrangement of 1-(N -Sulfonyl-1,2,3-triazol-4-yl)alkanols

Miura, Tomoya,Funakoshi, Yuuta,Morimoto, Masao,Biyajima, Tsuneaki,Murakami, Masahiro

supporting information, p. 17440 - 17443,4 (2012/12/12)

Enaminones are synthesized by the rhodium(II)-catalyzed denitrogenative rearrangement reaction of 1-(N-sulfonyl-1,2,3-triazol-4-yl)alkanols, which are readily prepared from propargylic alcohols and N-sulfonyl azides. Intramolecular 1,2-hydride (or -alkyl)

Efficient synthesis of 1-sulfonyl-1,2,3-triazoles

Raushel, Jessica,Fokin, Valery V.

supporting information; experimental part, p. 4952 - 4955 (2010/12/25)

An efficient room-temperature method for the synthesis of 1-sulfonyl-1,2,3-triazoles from in situ generated copper(I) acetylides and sulfonyl azides is described. The copper(I) thiophene-2-carboxylate (CuTC) catalyst produces the title compounds under both nonbasic anhydrous and aqueous conditions in good yields.

Copper-catalyzed cycloaddition of sulfonyl azides with alkynes to synthesize N-sulfonyltriazoles 'on water' at room temperature

Wang, Feng,Fu, Hua,Jiang, Yuyang,Zhao, Yufen

supporting information; experimental part, p. 1830 - 1834 (2009/07/09)

We have developed a green and practical method for the Huisgen cycloaddition of water-insoluble sulfonyl azides with alkynes 'on water' at room temperature under catalysis of the inexpensive catalyst system CuX/PhSMe, and addition of the ligand (thioaniso

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