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Nsc81386, also known as N-[4-(2-piperidin-1-ylethoxy)phenyl]-5-(trifluoromethyl)-1H-pyrazole-3-carboxamide, is a synthetic chemical compound belonging to the pyrazole family. It features a substituted piperidine group and has been researched for its potential pharmaceutical applications, particularly as a novel analgesic and anti-inflammatory agent. Some studies suggest that Nsc81386 may exhibit activity at the cannabinoid receptors, although further research is required to fully elucidate its pharmacological properties and therapeutic potential.

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  • 1,2-Hydrazinedicarboxylicacid, 1-methyl-, 1,2-bis(phenylmethyl) ester

    Cas No: 6002-83-1

  • USD $ 1.9-2.9 / Gram

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  • 6002-83-1 Structure
  • Basic information

    1. Product Name: Nsc81386
    2. Synonyms: Nsc81386;dibenzyl 1-Methylhydrazine-1,2-dicarboxylate;DIBENZYL 1-METHYL-1,2-HYDRAZINEDICARBOXYLATE
    3. CAS NO:6002-83-1
    4. Molecular Formula: C17H18N2O4
    5. Molecular Weight: 314.339
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6002-83-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.23g/cm3
    6. Refractive Index: 1.58
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Nsc81386(CAS DataBase Reference)
    10. NIST Chemistry Reference: Nsc81386(6002-83-1)
    11. EPA Substance Registry System: Nsc81386(6002-83-1)
  • 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: 6002-83-1(Hazardous Substances Data)

6002-83-1 Usage

Uses

Used in Pharmaceutical Industry:
Nsc81386 is used as a potential analgesic and anti-inflammatory agent due to its pyrazole derivative structure and possible activity at cannabinoid receptors. This makes it a candidate for the development of new treatments for pain and inflammation-related conditions.
Used in Research and Development:
In the field of medicinal chemistry and drug discovery, Nsc81386 serves as a subject for further research to better understand its pharmacological properties, mechanism of action, and potential therapeutic applications. This research can aid in the design of more effective and safer drugs targeting pain and inflammation.

Check Digit Verification of cas no

The CAS Registry Mumber 6002-83-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,0 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6002-83:
(6*6)+(5*0)+(4*0)+(3*2)+(2*8)+(1*3)=61
61 % 10 = 1
So 6002-83-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H18N2O4/c1-19(17(21)23-13-15-10-6-3-7-11-15)18-16(20)22-12-14-8-4-2-5-9-14/h2-11H,12-13H2,1H3,(H,18,20)

6002-83-1SDS

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 benzyl N-methyl-N-(phenylmethoxycarbonylamino)carbamate

1.2 Other means of identification

Product number -
Other names 1-methyl-1,2-dicarbobenzoxy-hydrazine

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:6002-83-1 SDS

6002-83-1Relevant articles and documents

Regioselective Oxidation of β-Hydroxyazo Compounds to β-Hydroxyazoxy Compounds and Its Application to Syntheses of Maniwamycins A and B

Nakata, Masaya,Kawazoe, Soichiro,Tamai, Tetsuro,Tatsuta, Kuniaki,Ishiwata, Hiroyuki,et al.

, p. 6095 - 6098 (2007/10/02)

A new preparation of β-hydroxyazo compounds and regioselectivities on their oxidation to β-hydroxyazoxy compounds have been described.A new synthesis of antifungal antibiotic maniwamycin A and the first synthesis of maniwamycin B by using this methodology

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