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4,4-dimethyl-2-[(E)-2-phenylethenyl]-4,5-dihydro-1,3-oxazole is a complex organic chemical compound with the molecular formula C13H15NO. It is a derivative of 1,3-oxazole, which is a heterocyclic compound containing oxygen and nitrogen atoms. The structure of 4,4-dimethyl-2-[(E)-2-phenylethenyl]-4,5-dihydro-1,3-oxazole features a 1,3-oxazole ring fused to a cyclohexane ring, with two methyl groups attached to the carbon atoms at positions 4 and 4', and a phenyl group connected to the carbon atom at position 2 through an E-configured double bond. 4,4-dimethyl-2-[(E)-2-phenylethenyl]-4,5-dihydro-1,3-oxazole is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as a building block in the development of new materials. Due to its unique structure and properties, it has attracted interest from researchers in the fields of organic chemistry and materials science.

1615-22-1

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1615-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1615-22-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1615-22:
(6*1)+(5*6)+(4*1)+(3*5)+(2*2)+(1*2)=61
61 % 10 = 1
So 1615-22-1 is a valid CAS Registry Number.

1615-22-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4-dimethyl-2-[(E)-2-phenylethenyl]-5H-1,3-oxazole

1.2 Other means of identification

Product number -
Other names 4,4-dimethyl-2-styryl-4,5-dihydro-oxazole

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:1615-22-1 SDS

1615-22-1Downstream Products

1615-22-1Relevant academic research and scientific papers

Use of Hypervalent Iodine in the Synthesis of Isomeric Dihydrooxazoles

Carlucci, Claudia,Tota, Arianna,Colella, Marco,Ronamazzi, Giuseppe,Clarkson, Guy J.,Luisi, Renzo,Degennaro, Leonardo

, p. 428 - 436 (2018/06/11)

[Figure not available: see fulltext.] A convenient synthesis of 2- and/or 3-oxazolines has been developed depending on the structure and stereochemistry of the starting amino alcohol. PhI(OAc)2 acted as oxidant on the intermediate imine, as sup

Open vessel mode microwave-assisted synthesis of 2-oxazolines from carboxylic acids

Sharma, Rishi,Vadivel, Subramanian K.,Duclos Jr., Richard I.,Makriyannis, Alexandros

experimental part, p. 5780 - 5782 (2009/12/26)

Microwave-assisted synthesis of 2-oxazolines from carboxylic acids using the open vessel technique is described. This efficient method involves direct condensation of carboxylic acids with excess 2-amino-2-methyl-1-propanol at 170 °C to give the corresponding 2-oxazolines in moderate to excellent yields.

Efficient oxidative conversion of aldehydes to 2-substituted oxazolines and oxazines using (diacetoxyiodo)benzene

Karade, Nandkishor N.,Tiwari, Girdharilal B.,Gampawar, Sumit V.

, p. 1921 - 1924 (2008/03/27)

An efficient synthesis of 2-substituted oxazolines from aldehydes and 2-amino alcohol using (diacetoxyiodo)benzene as an oxidant, is reported. (Diacetoxyiodo)benzene acts as a mild dehydrogenating agent to convert the initially formed oxazolidine from ald

Facile Syntheses of Oxazolines and Thiazolines with N-Acylbenzotriazoles under Microwave Irradiation

Katritzky, Alan R.,Cai, Chunming,Suzuki, Kazuyuki,Singh, Sandeep K.

, p. 811 - 814 (2007/10/03)

Microwave reactions of 2-amino-2-methyl-1-propanol (2) or 2-aminoethanethiol hydrochloride (4) with readily available N-acylbenzotriazoles 1a-j in the presence of SOCl2 produced 2-substituted 2-oxazolines 3a-j in 84-98% yields and 2-substituted

Reactions of 2-(Tributylstannyl)-4,4-dimethyl-2-oxazoline with Organic Halides. Unusual Product from Aroyl Halide

Kosugi, Masanori,Fukiage, Akio,Takayanagi, Mitsuhiro,Sano, Hiroshi,Migita, Toshihiko,Satoh, Mitsuo

, p. 1351 - 1354 (2007/10/02)

2-(Tributylstannyl)-4,4-dimethyl-2-oxazoline (1) reacted with aroyl chloride smoothly without any palladium catalyst to give the unusual product, bis(N-aroyl-4,4-dimethyl-2-oxazolinylidene) in good yields.The reaction of 1 with other types of halide neede

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