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30650-90-9

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30650-90-9 Usage

General Description

ETHYL 3-METHYL-4-NITROBENZOATE is an organic compound with the molecular formula C10H11NO4. It is an ester, characterized by the presence of an ethyl group attached to the carboxyl group of 3-methyl-4-nitrobenzoic acid. This chemical is commonly used in the manufacturing of perfumes and flavorings due to its pleasant odor. It is also utilized in the production of pharmaceuticals and as an intermediate in organic synthesis. ETHYL 3-METHYL-4-NITROBENZOATE is considered to have low toxicity and is not expected to be harmful if used and handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 30650-90-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,5 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 30650-90:
(7*3)+(6*0)+(5*6)+(4*5)+(3*0)+(2*9)+(1*0)=89
89 % 10 = 9
So 30650-90-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO4/c1-3-15-10(12)8-4-5-9(11(13)14)7(2)6-8/h4-6H,3H2,1-2H3

30650-90-9 Well-known Company Product Price

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  • Alfa Aesar

  • (A18625)  Ethyl 3-methyl-4-nitrobenzoate, 98%   

  • 30650-90-9

  • 10g

  • 107.0CNY

  • Detail
  • Alfa Aesar

  • (A18625)  Ethyl 3-methyl-4-nitrobenzoate, 98%   

  • 30650-90-9

  • 50g

  • 424.0CNY

  • Detail
  • Alfa Aesar

  • (A18625)  Ethyl 3-methyl-4-nitrobenzoate, 98%   

  • 30650-90-9

  • 250g

  • 1792.0CNY

  • Detail

30650-90-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 3-METHYL-4-NITROBENZOATE

1.2 Other means of identification

Product number -
Other names 3-Methyl-4-nitro-benzoesaeure-aethylester

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:30650-90-9 SDS

30650-90-9Relevant articles and documents

Oxygen-Tolerant H2 Production by [FeFe]-H2ase Active Site Mimics Aided by Second Sphere Proton Shuttle

Ahmed, Md Estak,Dey, Subal,Darensbourg, Marcetta Y.,Dey, Abhishek

, p. 12457 - 12468 (2018)

The instability of [FeFe]-H2ases and their biomimetics toward O2 renders them inefficient to implement in practical H2 generation (HER). Previous investigations on synthetic models as well as natural enzymes proved that re

Synthesis of symmetric diester-functionalised Troeger's base analogues

Bhuiyan, M. Delower H.,Zhu, Kai-Xian,Jensen, Paul,Try, Andrew C.

supporting information; experimental part, p. 4662 - 4670 (2010/10/19)

The yields of ester-functionalised Troeger's base analogues are dramatically improved by incorporating an electron-donating group on the aromatic ring and/or enhancing solubil- ity of the aniline unit. In addition to 2,8-diester compounds, 1,7-, 3,9- and 4,10-diester-functionalised Troeger's base analogues have been prepared for the first time.

Integrin antagonists

-

, (2008/06/13)

This invention relates to novel heterocycles which are useful as antagonists of the αvβ3 integrin, the α2bβ3 integrin, and related cell surface adhesive protein receptors, to pharmaceutical compositions containing such compounds, processes for preparing such compounds, and to methods of using these compounds, alone or in combination with other therapeutic agents, for the inhibition of cell adhesion, the treatment of angiogenic disorders, inflammation, bone degradation, cancer metastasis, diabetic retinopathy, thrombosis, restenosis, macular degeneration, and other conditions mediated by cell adhesion and/or cell migration and/or angiogenesis.

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