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91215-03-1

4-({5-nitro-2-methylphenyl}sulfonyl)morpholine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 91215-03-1 Structure

  • Basic information

    1. Product Name: 4-({5-nitro-2-methylphenyl}sulfonyl)morpholine
    2. Synonyms: 4-({5-nitro-2-methylphenyl}sulfonyl)morpholine
    3. CAS NO:91215-03-1
    4. Molecular Formula: C11H14N2O5S
    5. Molecular Weight: 286.30426
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 91215-03-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-({5-nitro-2-methylphenyl}sulfonyl)morpholine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-({5-nitro-2-methylphenyl}sulfonyl)morpholine(91215-03-1)
    11. EPA Substance Registry System: 4-({5-nitro-2-methylphenyl}sulfonyl)morpholine(91215-03-1)

  • 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: 91215-03-1(Hazardous Substances Data)

91215-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91215-03-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,1 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91215-03:
(7*9)+(6*1)+(5*2)+(4*1)+(3*5)+(2*0)+(1*3)=101
101 % 10 = 1
So 91215-03-1 is a valid CAS Registry Number.

91215-03-1Relevant articles and documents

Novel sulfamoyl benzamides as selective CB2 agonists with improved in vitro metabolic stability

Sellitto, Ian,Bourdonnec, Bertrand Le,Worm, Karin,Goodman, Allan,Savolainen, Markku A.,Chu, Guo-Hua,Ajello, Christopher W.,Saeui, Christopher T.,Leister, Lara K.,Cassel, Joel A.,DeHaven, Robert N.,LaBuda, Christopher J.,Koblish, Michael,Little, Patrick J.,Brogdon, Bernice L.,Smith, Steven A.,Dolle, Roland E.

scheme or table, p. 387 - 391 (2010/04/06)

A lead optimization campaign in our previously reported sulfamoyl benzamide class of CB2 agonists was conducted to improve the in vitro metabolic stability profile in this series while retaining high potency and selectivity for the CB2 receptor. From this study, compound 14, N-(3,4-dimethyl-5-(morpholinosulfonyl)phenyl)-2,2-dimethylbutanamide, was identified as a potent and selective CB2 agonist exhibiting moderate in vitro metabolic stability and oral bioavailability. Compound 14 demonstrated in vivo efficacy in a rat model of post-surgical pain.

CB2 selective sulfamoyl benzamides: Optimization of the amide functionality

Goodman, Allan J.,Ajello, Christopher W.,Worm, Karin,Bourdonnec, Bertrand Le,Savolainen, Markku A.,O'Hare, Heather,Cassel, Joel A.,Stabley, Gabriel J.,DeHaven, Robert N.,LaBuda, Christopher J.,Koblish, Michael,Little, Patrick J.,Brogdon, Bernice L.,Smith, Steven A.,Dolle, Roland E.

scheme or table, p. 309 - 313 (2011/02/26)

Previous research within our laboratories identified sulfamoyl benzamides as novel cannabinoid receptor ligands. Optimization of the amide linkage led to the reverse amide 40. The compound exhibited robust antiallodynic activity in a rodent pain model whe

PYRIMIDINES, TRIAZINES AND THEIR USE AS PHARMACEUTICAL AGENTS

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Page/Page column 37, (2009/10/22)

A compound of formula (I) and its pharmaceutically acceptable salts or solvates and physiologically hydrolysable, solubilising or immobilisable derivatives wherein: Ar is a 5-membered heteroaryl ring wherein X1 and X2 are one or two

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