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(2E)-1-phenyl-3-[3-(phenylamino)-4-thia-1,2-diazaspiro[4.5]dec-2-en-1-yl]prop-2-en-1-one is a complex organic compound with a molecular formula of C24H22N2OS. It is a yellow solid that is soluble in organic solvents and is commonly used as a building block for the synthesis of various pharmaceuticals and fine chemicals. (2E)-1-phenyl-3-[3-(phenylamino)-4-thia-1,2-diazaspiro[4.5]dec-2-en-1-yl]prop-2-en-1-one contains a spiro[4.5]dec-2-en-1-yl moiety, which is a bicyclic heterocyclic ring system, and a phenylamino group, which imparts unique chemical and biological properties. It is known for its diverse range of pharmacological activities, including antifungal, antimicrobial, and antiproliferative effects, making it a valuable target for medicinal chemistry research and drug development.

125810-87-9

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125810-87-9 Usage

Uses

Used in Pharmaceutical Industry:
(2E)-1-phenyl-3-[3-(phenylamino)-4-thia-1,2-diazaspiro[4.5]dec-2-en-1-yl]prop-2-en-1-one is used as a building block for the synthesis of various pharmaceuticals and fine chemicals. Its unique chemical and biological properties, including antifungal, antimicrobial, and antiproliferative effects, make it a valuable target for medicinal chemistry research and drug development.
Used in Medicinal Chemistry Research:
(2E)-1-phenyl-3-[3-(phenylamino)-4-thia-1,2-diazaspiro[4.5]dec-2-en-1-yl]prop-2-en-1-one is used as a valuable target for medicinal chemistry research due to its diverse range of pharmacological activities. Its unique chemical and biological properties make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Fine Chemicals Industry:
(2E)-1-phenyl-3-[3-(phenylamino)-4-thia-1,2-diazaspiro[4.5]dec-2-en-1-yl]prop-2-en-1-one is used as a building block for the synthesis of various fine chemicals. Its unique chemical and biological properties make it a valuable component in the development of specialty chemicals and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 125810-87-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,8,1 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 125810-87:
(8*1)+(7*2)+(6*5)+(5*8)+(4*1)+(3*0)+(2*8)+(1*7)=119
119 % 10 = 9
So 125810-87-9 is a valid CAS Registry Number.

125810-87-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(2-anilino-1-thia-3,4-diazaspiro[4.5]dec-2-en-4-yl)-1-phenylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names (E)-3-(3-anilino-4-thia-1,2-diazaspiro[4.5]dec-2-en-1-yl)-1-phenylprop-2-en-1-one

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:125810-87-9 SDS

125810-87-9Downstream Products

125810-87-9Relevant academic research and scientific papers

THE REACTION OF TERMINAL α-ACETYLENIC KETONES WITH THIOSEMICARBAZONES

Komarova, T. N.,Nakhmanovich, A. S.,Sigalov, M. V.,Glotova, T. E.

, p. 1058 - 1060 (2007/10/02)

The reaction of terminal α-acetylenic ketones with thiosemicarbazones gives a series of 5-amino- and 5-anilino-3-acylvinyl-Δ4-1,3,4-thiadiazolines.These products react with perchloric acid to give the corresponding perchlorates.

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