Welcome to LookChem.com Sign In|Join Free
  • or
Propan-2-yl (3-nitrophenyl)carbamate is an organic compound with the chemical formula C10H12N2O4. It is a derivative of carbamic acid, where the hydrogen atom is replaced by a propyl group and a 3-nitrophenyl group. propan-2-yl (3-nitrophenyl)carbamate is characterized by its molecular structure, which includes a carbamate functional group, a nitro group attached to a phenyl ring, and a three-carbon propyl chain. It is a colorless to pale yellow solid and is soluble in organic solvents. Propan-2-yl (3-nitrophenyl)carbamate is used in the synthesis of various pharmaceuticals and agrochemicals due to its reactivity and the ability to form esters with carboxylic acids. It is also known for its potential applications in the development of new materials and as an intermediate in chemical reactions.

2610-62-0

Post Buying Request

2610-62-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2610-62-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2610-62-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,1 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2610-62:
(6*2)+(5*6)+(4*1)+(3*0)+(2*6)+(1*2)=60
60 % 10 = 0
So 2610-62-0 is a valid CAS Registry Number.

2610-62-0SDS

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 propan-2-yl N-(3-nitrophenyl)carbamate

1.2 Other means of identification

Product number -
Other names -

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:2610-62-0 SDS

2610-62-0Relevant academic research and scientific papers

Effect of successive increase in alcohol chains on reaction with isocyanates and isothiocyanates

Perveen, Shahnaz,Yasmin, Arfa,Khan, Khalid Mohammed

experimental part, p. 18 - 23 (2010/04/23)

The reaction of isocyanates and isothiocyanates with long-chain alcohols, e.g. n-hexanol, n-heptanol and n-octanol, exclusively gave N-aryl-O-alkyl carbamates, while N-aryl-O-alkyl carbamates were formed along with symmetrical 1,3-disubstituted ureas and thioureas when the same reactions were carried out with small-chain alcohols at room temperature without using any solvent.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 2610-62-0