Welcome to LookChem.com Sign In|Join Free

CAS

  • or

565448-32-0

Methanesulfonamide, N-[3-(azidomethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

565448-32-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 565448-32-0 Structure

  • Basic information

    1. Product Name: Methanesulfonamide, N-[3-(azidomethyl)phenyl]-
    2. Synonyms:
    3. CAS NO:565448-32-0
    4. Molecular Formula: C8H10N4O2S
    5. Molecular Weight: 226.259
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 565448-32-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Methanesulfonamide, N-[3-(azidomethyl)phenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methanesulfonamide, N-[3-(azidomethyl)phenyl]-(565448-32-0)
    11. EPA Substance Registry System: Methanesulfonamide, N-[3-(azidomethyl)phenyl]-(565448-32-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 565448-32-0(Hazardous Substances Data)

565448-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 565448-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,5,4,4 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 565448-32:
(8*5)+(7*6)+(6*5)+(5*4)+(4*4)+(3*8)+(2*3)+(1*2)=180
180 % 10 = 0
So 565448-32-0 is a valid CAS Registry Number.

565448-32-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[3-(azidomethyl)phenyl]methanesulfonamide

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:565448-32-0 SDS

565448-32-0Relevant articles and documents

N-(3-acyloxy-2-benzylpropyl)-N′-[4-(methylsulfonylamino)benzyl]thiourea analogues: Novel potent and high affinity antagonists and partial antagonists of the vanilloid receptor

Lee, Jeewoo,Lee, Jiyoun,Kang, Myungshim,Shin, Myoungyoup,Kim, Ji-Min,Kang, Sang-Uk,Lim, Ju-Ok,Choi, Hyun-Kyung,Suh, Young-Ger,Park, Hyeung-Geun,Oh, Uhtaek,Kim, Hee-Doo,Park, Young-Ho,Ha, Hee-Jin,Kim, Young-Ho,Toth, Attila,Wang, Yun,Tran, Richard,Pearce, Larry V.,Lundberg, Daniel J.,Blumberg, Peter M.

, p. 3116 - 3126 (2007/10/03)

Isosteric replacement of the phenolic hydroxyl group in potent vanilloid receptor (VR1) agonists with the alkylsulfonamido group provides a series of compounds which are effective antagonists to the action of the capsaicin on rat VR1 heterologously expressed in Chinese hamster ovary (CHO) cells. In particular, compound 61, N-[2-(3,4-dimethylbenzyl)-3-pivaloyloxypropyl]-N′-[3-fluoro-4- (methylsulfonylamino)benzyl]thiourea was a full antagonist against capsaicin, displayed a Ki value of 7.8 nM (compared to 520 nM for capsazepine and 4 nM for 5-iodoRTX), and showed excellent analgesic activity in mice. Structure-activity analysis of the influence of modifications in the A- and C-regions of 4-methylsulfonamide ligands on VR1 agonism/antagonism indicated that 3-fluoro substitution in the A-region and a 4-tert-butylbenzyl moiety in the C-region favored antagonism, whereas a 3-methoxy group in the A-region and 3-acyloxy2-benzylpropyl moieties in the C-region favored agonism.

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

What can I do for you?
Get Best Price

Get Best Price for 565448-32-0