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59382-60-4

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59382-60-4 Usage

General Description

Ethyl 2-methyl-3-nitrobenzoate is a chemical compound with the molecular formula C10H11NO4. It is a yellow crystalline solid that is commonly used in the production of fragrances and flavoring agents. Ethyl 2-methyl-3-nitrobenzoate is commonly used in the manufacturing of perfumes and as a flavoring agent in the food industry. It is also used in organic synthesis as a source of 2-methyl-3-nitrobenzoic acid, which is a building block for a variety of pharmaceuticals and agrochemicals. However, it is important to handle this compound with caution as it is toxic if ingested, inhaled, or comes into contact with the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 59382-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,3,8 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59382-60:
(7*5)+(6*9)+(5*3)+(4*8)+(3*2)+(2*6)+(1*0)=154
154 % 10 = 4
So 59382-60-4 is a valid CAS Registry Number.

59382-60-4SDS

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 2-methyl-3-nitrobenzoate

1.2 Other means of identification

Product number -
Other names Ethyl 2-methyl-3-nitro-benzoat

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:59382-60-4 SDS

59382-60-4Relevant articles and documents

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.

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