Welcome to LookChem.com Sign In|Join Free
  • or
N-(3-chloropropyl)methanesulfonamide is a chemical compound with the molecular formula C4H10ClNO2S. It is a sulfonamide compound with a chloropropyl group attached to the nitrogen atom. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also known to have antimicrobial and antifungal properties, making it useful in the development of antimicrobial agents. Additionally, N-(3-chloropropyl)methanesulfonamide has been studied for its potential application in the treatment of cancer, as it has shown promising anti-proliferative effects on cancer cells in vitro. Overall, N-(3-chloropropyl)methanesulfonamide has diverse applications in the fields of pharmaceuticals, agrochemicals, and medical research.

57590-72-4

Post Buying Request

57590-72-4 Suppliers

Recommended suppliers

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

57590-72-4 Usage

Uses

Used in Pharmaceutical Industry:
N-(3-chloropropyl)methanesulfonamide is used as an intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into the structure of different drugs.
Used in Agrochemical Industry:
N-(3-chloropropyl)methanesulfonamide is used as an intermediate in the synthesis of various agrochemicals to help develop new pesticides or other agricultural products.
Used in Antimicrobial Applications:
N-(3-chloropropyl)methanesulfonamide is used as an antimicrobial agent due to its antimicrobial and antifungal properties, which can be utilized in the development of treatments for infections.
Used in Cancer Research and Treatment:
N-(3-chloropropyl)methanesulfonamide is used in medical research as a potential anti-cancer agent for its demonstrated anti-proliferative effects on cancer cells in vitro, indicating its potential use in the development of cancer therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 57590-72-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,9 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57590-72:
(7*5)+(6*7)+(5*5)+(4*9)+(3*0)+(2*7)+(1*2)=154
154 % 10 = 4
So 57590-72-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H10ClNO2S/c1-9(7,8)6-4-2-3-5/h6H,2-4H2,1H3

57590-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3-chloropropyl)methanesulfonamide

1.2 Other means of identification

Product number -
Other names N-(3-chloropropyl)-methanesulfonamide

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:57590-72-4 SDS

57590-72-4Downstream Products

57590-72-4Relevant academic research and scientific papers

PYRAZOLE COMPOUNDS AS JAK INHIBITORS

-

Page/Page column 38, (2011/11/13)

The present invention relates to compounds of formula (I), wherein R1, R2, R1a, R1b have the meaning as cited in the description and the claims. Said compounds are useful as JAK inhibitors for the treatment or prophylaxis of immunological, inflammatory, autoimmune, allergic disorders, and immunologically-mediated diseases. The invention also relates to pharmaceutical compositions including said compounds, the preparation of such compounds as well as the use as medicaments.

Practical Synthesis of Sultams via Sulfonamide Dianion Alkylation: Application to the Synthesis of Chiral Sultams

Lee, Jaemoon,Zhong, Yong-Li,Reamer, Robert A.,Askin, David

, p. 4175 - 4177 (2007/10/03)

(Equation presented) A practical synthesis of sultams was developed via intramolecular sulfonamide dianion alkylation. This method has been applied toward the synthesis of chiral sultams, which are synthetically valuable as chiral auxiliaries.

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 57590-72-4