2613-76-5 Usage
Description
1H-INDENE,2,3-DIHYDRO-1,1,3-T, with the chemical formula C9H10, is a colorless liquid known for its sweet, floral odor. This chemical compound is recognized for its versatility in various industrial applications, primarily as a flavoring agent in the food industry and in the production of fragrances and perfumes. It also serves as an intermediate in the synthesis of other chemicals and pharmaceuticals. However, due to its potential health hazards, it is crucial to handle 1H-INDENE,2,3-DIHYDRO-1,1,3-T with caution and follow proper safety protocols.
Uses
Used in Food Industry:
1H-INDENE,2,3-DIHYDRO-1,1,3-T is used as a flavoring agent for its distinctive sweet, floral scent, enhancing the taste and aroma of various food products.
Used in Fragrance and Perfume Industry:
This chemical compound is utilized in the production of fragrances and perfumes, contributing to the creation of complex and appealing scents for a wide range of consumer products.
Used in Chemical Synthesis:
1H-INDENE,2,3-DIHYDRO-1,1,3-T serves as an intermediate in the synthesis of other chemicals, playing a crucial role in the development of new compounds and materials.
Used in Pharmaceutical Industry:
As an intermediate, 1H-INDENE,2,3-DIHYDRO-1,1,3-T is also involved in the synthesis of pharmaceuticals, aiding in the production of various medications and treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 2613-76-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,1 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2613-76:
(6*2)+(5*6)+(4*1)+(3*3)+(2*7)+(1*6)=75
75 % 10 = 5
So 2613-76-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H16/c1-9-8-12(2,3)11-7-5-4-6-10(9)11/h4-7,9H,8H2,1-3H3
2613-76-5Relevant articles and documents
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Pines,Postl
, p. 1769 (1957)
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Formylation and Acylation Reactions Catalysed by Trifluoromethanesulphonic Acid
Booth, Brian L.,El-Fekky, Teymour A.,Noori, Ghazi F. M.
, p. 181 - 186 (2007/10/02)
Regioselective formylation of toluene, m- and p-xylene, and mesitylene has been achieved by carbonylation in trifluoromethanesulphonic acid at CO pressures of 90-125 atm.In the case of cumene, the formylation reaction is in competition with disproportionation to form di- and tri-isopropylbenzenes, leading to a complex product mixture.Slow addition of cyclohexene or cyclopentene to a mixture of benzene and CF3SO3H under a high CO pressure affords 4-cyclohexylbenzaldehyde and 4-cyclopentylbenzaldehyde in 34percent and 33percent yieds, respectively, while 2-methylbut-1-ene gives 2,2,3-trimethylindanone (39percent) under similar conditions.When cyclohexene is mixed with the acid under carbon monoxide (120 atm) before addition of benzene the major products are cyclohexyl phenyl ketone and cyclohexenyl cyclohexyl ketones.
