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acide cis-N-tosyl perhydrocyclopentapyrrole-2-carboxylique is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134786-35-9

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  • 134786-35-9 Structure

  • Basic information

    1. Product Name: acide cis-N-tosyl perhydrocyclopentapyrrole-2-carboxylique
    2. Synonyms:
    3. CAS NO:134786-35-9
    4. Molecular Formula:
    5. Molecular Weight: 309.386
    6. EINECS: N/A
    7. Product Categories: N/A

  • 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: acide cis-N-tosyl perhydrocyclopentapyrrole-2-carboxylique(CAS DataBase Reference)
    10. NIST Chemistry Reference: acide cis-N-tosyl perhydrocyclopentapyrrole-2-carboxylique(134786-35-9)
    11. EPA Substance Registry System: acide cis-N-tosyl perhydrocyclopentapyrrole-2-carboxylique(134786-35-9)

  • 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: 134786-35-9(Hazardous Substances Data)

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134786-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134786-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,7,8 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 134786-35:
(8*1)+(7*3)+(6*4)+(5*7)+(4*8)+(3*6)+(2*3)+(1*5)=149
149 % 10 = 9
So 134786-35-9 is a valid CAS Registry Number.

134786-35-9Downstream Products

134786-35-9Relevant academic research and scientific papers

Synthesis of 2,3-dihydro-1: H -pyrroles by intramolecular cyclization of N -(3-butynyl)-sulfonamides

Chung, Min-Ching,Chan, Yung-Hsiang,Chang, Wen-Jung,Hou, Duen-Ren

, p. 3783 - 3790 (2017/07/07)

Hydroamination of 3-butynamine derivatives to give non-aromatic 2,3-dihydropyrroles was achieved by using PdCl2 or AuCl as the catalyst. With microwave-assisted heating, up to 92% isolated yield was obtained from this intramolecular 5-endo-dig

CYCLISATION DE N-TOSYL OXIRANES-PROPYLAMINES: SYNTHESE D'HETEROCYCLES AZOTES.

Nuhrich, A.,Moulines, J.

, p. 3075 - 3088 (2007/10/02)

The cyclisation of N-tosyl-oxiranepropylamines is accomplished in aqueous basic medium and in anhydrous acid medium as well.In most cases, this reaction occurs by a regiospecific 5-exo-tet. ring closure and affords N-tosyl-2-pyrrolidinemethanols in high y

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