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3-Pentanone, 2-(3,4-dimethoxyphenyl)-, also known as 2-(3,4-dimethoxyphenyl)pentan-3-one, is an organic compound with the molecular formula C11H16O3. It is a colorless liquid with a molecular weight of 192.24 g/mol. This chemical is characterized by the presence of a pentanone functional group (a ketone with a five-carbon chain) and a 3,4-dimethoxyphenyl group, which consists of a benzene ring with two methoxy groups attached at the 3rd and 4th positions. 3-Pentanone, 2-(3,4-dimethoxyphenyl)- is used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is important to handle this chemical with care, as it may have potential health risks and should be stored and used according to proper safety guidelines.

92156-84-8

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92156-84-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92156-84-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,5 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92156-84:
(7*9)+(6*2)+(5*1)+(4*5)+(3*6)+(2*8)+(1*4)=138
138 % 10 = 8
So 92156-84-8 is a valid CAS Registry Number.

92156-84-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4-Dimethoxyphenyl)-3-pentanone

1.2 Other means of identification

Product number -
Other names Oxirane,(3,4-dimethoxyphenyl)

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:92156-84-8 SDS

92156-84-8Relevant academic research and scientific papers

Synthesis of substituted isoquinolines via Pd-catalyzed cross-coupling approaches

Todorovic, Nick,Awuah, Emelia,Albu, Silvia,Ozimok, Cory,Capretta, Alfredo

supporting information; experimental part, p. 6180 - 6183 (2012/01/03)

Palladium complexes incorporating ligands based on a 1,3,5,7-tetramethyl-2, 4,8-trioxa-6-phosphaadamantanyl scaffold were used to catalyze the arylation of ethyl cyanoacetate, malononitrile, and various ketones. The products from these reactions can be el

Use of conjugated dienones in cyclialkylations: Total syntheses of arucadiol, 1,2-didehydromiltirone, (±)-hinokione, (±)-nimbidiol, sageone, and miltirone

Majetich, George,Liu, Shuang,Fang, Jing,Siesel, David,Zhang, Yong

, p. 6928 - 6951 (2007/10/03)

Functionalized hydrophenanthrenes can be prepared using a cyclialkylation-based strategy. These annulations are highly dependent on the directing effects of the arene substitutents and on conformational considerations. The utility of this methodology was featured in the syntheses of six diterpenoids.

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