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5-methyl-7-phenyl-2,3-dihydro-1H-pyrrolizine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 291276-01-2 Structure
  • Basic information

    1. Product Name: 5-methyl-7-phenyl-2,3-dihydro-1H-pyrrolizine
    2. Synonyms: 5-methyl-7-phenyl-2,3-dihydro-1H-pyrrolizine
    3. CAS NO:291276-01-2
    4. Molecular Formula:
    5. Molecular Weight: 197.28
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 291276-01-2.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: 5-methyl-7-phenyl-2,3-dihydro-1H-pyrrolizine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-methyl-7-phenyl-2,3-dihydro-1H-pyrrolizine(291276-01-2)
    11. EPA Substance Registry System: 5-methyl-7-phenyl-2,3-dihydro-1H-pyrrolizine(291276-01-2)
  • 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: 291276-01-2(Hazardous Substances Data)

291276-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 291276-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,1,2,7 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 291276-01:
(8*2)+(7*9)+(6*1)+(5*2)+(4*7)+(3*6)+(2*0)+(1*1)=142
142 % 10 = 2
So 291276-01-2 is a valid CAS Registry Number.

291276-01-2Upstream product

291276-01-2Downstream Products

291276-01-2Relevant articles and documents

A facile synthesis of polysubstituted pyrroles

Dieter, R. Karl,Yu, Huayun

, p. 2283 - 2286 (2000)

(equation presented) α-Aminoalkylcuprates prepared from CuX·2LiCI (X = Cl, CN) and 1 equiv of an α-lithiocarbamate undergo conjugate addition reactions to α,β-alkynyl ketones in moderate to good yields, affording E:Z mixtures of α,β-enones. Treatment of the conjugate adducts with PhOH/TMSCI in CH2CI2 effected carbamate deprotection and cyclization to afford a flexible two-step synthesis of substituted pyrroles.

FUSED PYRROLE COMPOUNDS, PHARMACEUTICAL AGENTS CONTAINING THE SAME, AND THE USE THEREOF

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Page 46, (2010/02/04)

The present invention relates to fused pyrrole compounds of the formula 1. in which at least one of the radicals R1, R2, R3 is 4-sulphur-substituted phenyl. These compounds are in particular pyrrolizines, indolizines and heteroanalogues having selective inhibitory action on isoenzyme-2 of prostaglandin H synthase (COX-2). The invention also relates to pharmaceutical compositions which contain these compounds; and the use of these compounds for the treatment of disorders of the rheumatic type.

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