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Benzenecarboximidic acid, 3,4-dimethyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55308-45-7

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55308-45-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55308-45-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,0 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55308-45:
(7*5)+(6*5)+(5*3)+(4*0)+(3*8)+(2*4)+(1*5)=117
117 % 10 = 7
So 55308-45-7 is a valid CAS Registry Number.

55308-45-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3,4-dimethylbenzenecarboximidate

1.2 Other means of identification

Product number -
Other names Benzenecarboximidic acid,3,4-dimethyl-,ethyl ester

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:55308-45-7 SDS

55308-45-7Relevant academic research and scientific papers

Synthesis of 1H-Indazoles from Imidates and Nitrosobenzenes via Synergistic Rhodium/Copper Catalysis

Wang, Qiang,Li, Xingwei

, p. 2102 - 2105 (2016)

Nitrosobenzenes have been used as a convenient aminating reagent for the efficient synthesis of 1H-indazoles via rhodium and copper catalyzed C-H activation and C-N/N-N coupling. The reaction occurred under redox-neutral conditions with high efficiency and functional group tolerance. Moreover, a rhodacyclic imidate complex has been identified as a key intermediate.

Rh(III)-Catalyzed C-C/C-N Coupling of Imidates with α-Diazo Imidamide: Synthesis of Isoquinoline-Fused Indoles

Wang, He,Li, Lei,Yu, Songjie,Li, Yunyun,Li, Xingwei

supporting information, p. 2914 - 2917 (2016/07/06)

Imidate esters and diazo compounds have been established as bifunctional substrates for the construction of biologically active fused heterocycles via rhodium-catalyzed C-H activation and C-C/C-N coupling. This reaction occurs under mild conditions with high efficiency, step economy, and low catalyst loading.

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