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1-Propen-2-amine, 1-[3-(4-chlorophenyl)-1,2,4-thiadiazol-5-yl]- is a complex organic chemical compound with the molecular formula C9H8ClN3S2. It is a derivative of 1-propen-2-amine, featuring a 1,2,4-thiadiazol-5-yl group attached to the nitrogen atom. The 1,2,4-thiadiazol-5-yl group itself contains a 4-chlorophenyl substituent, which adds to the compound's structural complexity. 1-Propen-2-amine, 1-[3-(4-chlorophenyl)-1,2,4-thiadiazol-5-yl]- is characterized by its amine and thiadiazole functionalities, which may contribute to its potential reactivity and applications in various chemical processes. The presence of the chlorine atom on the phenyl ring can influence its chemical properties, such as reactivity and solubility. Overall, 1-Propen-2-amine, 1-[3-(4-chlorophenyl)-1,2,4-thiadiazol-5-yl]- represents a specific class of organic molecules that could be relevant in the fields of pharmaceuticals, agrochemicals, or materials science, depending on its specific properties and reactivity.

88090-93-1

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88090-93-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88090-93-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,9 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88090-93:
(7*8)+(6*8)+(5*0)+(4*9)+(3*0)+(2*9)+(1*3)=161
161 % 10 = 1
So 88090-93-1 is a valid CAS Registry Number.

88090-93-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-(4-chlorophenyl)-1,2,4-thiadiazol-5-yl]prop-1-en-2-amine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:88090-93-1 SDS

88090-93-1Downstream Products

88090-93-1Relevant academic research and scientific papers

RING-TRANSFORMATION EQUILIBRIUM WITH PARTICIPATION OF ?-BONDED S(IV) IN AN ISOTHIAZOLE SYSTEM. SYNTHESIS OF NON-RING-TRANSFORMED 5-(2-AMINOVINYL)ISOTHIAZOLE DERIVATIVE VIA 1,3-SILYL GROUP SHIFT

Ohkata, Katsuo,Ohyama, Yoshihiko,Watanabe, Yuko,Akiba, Kin-ya

, p. 4561 - 4564 (2007/10/02)

Substituents at 5-position of 5-amino-3-methyl- and 3-p-chlorophenyl-5-methylisothiazoles (7 and 8) were silylated and then lithiated to couple with aromatic nitriles in order to afford the adducts (4 and 5) via 1,3-silyl group shift.Desilylation of 5 wit

RING-TRANSFORMATION FROM ISOTHIAZOLE TO 1,2,4-THIADIAZOLE - POSSIBLE INTERMEDIACY OF ?-SULFURANE

Akiba, Kin-Ya,Noda, Akiko,Ohkata, Katsuo

, p. 111 - 118 (2007/10/02)

5-Amino-3-methyl- and 5-amino-3-phenylisothiazoles (3a and 3b) afforded 1:1 adducts with aromatic nitriles and imidates.On the basis of their spectral data and the structure of hydrolysis products, the adducts were identified as 3-substituted 5-(2-aminovinyl)-1,2,4-thiadiazole derivatives (2a-g), where ring transformation took place from isothiazole to 1,2,4-thiadiazole.

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