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N-(cyclopent-2-en-1-yl)-2-iodo-4,6-dimethylaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1421238-40-5 Structure
  • Basic information

    1. Product Name: N-(cyclopent-2-en-1-yl)-2-iodo-4,6-dimethylaniline
    2. Synonyms:
    3. CAS NO:1421238-40-5
    4. Molecular Formula:
    5. Molecular Weight: 313.181
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1421238-40-5.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: N-(cyclopent-2-en-1-yl)-2-iodo-4,6-dimethylaniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(cyclopent-2-en-1-yl)-2-iodo-4,6-dimethylaniline(1421238-40-5)
    11. EPA Substance Registry System: N-(cyclopent-2-en-1-yl)-2-iodo-4,6-dimethylaniline(1421238-40-5)
  • 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: 1421238-40-5(Hazardous Substances Data)

1421238-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1421238-40-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,1,2,3 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1421238-40:
(9*1)+(8*4)+(7*2)+(6*1)+(5*2)+(4*3)+(3*8)+(2*4)+(1*0)=115
115 % 10 = 5
So 1421238-40-5 is a valid CAS Registry Number.

1421238-40-5Downstream Products

1421238-40-5Relevant articles and documents

Synthesis of N-acetyl-3,3a,4,8b- and -1,3a,4,8b-tetrahydrocyclopenta[b] indoles from N- and 2-(cyclopent-2-en-1-yl)anilines

Skladchikov,Buranbaeva,Fatykhov,Ivanov,Gataullin

, p. 1550 - 1556 (2012)

Reactions of 2-bromo-N-(cyclopent-2-en-1-yl)-4-methylaniline and N-(cyclopent-2-en-1-yl)-2-iodo-4,6-dimethylaniline with acetyl bromide in the presence of potassium carbonate gave mixtures of syn and anti atropisomers of the corresponding N-acetyl derivatives at ratios of 1: 1 and 3: 2 respectively. Heating of these mixtures in toluene in the presence of Pd(OAc)2, PPh3, Et3N, and K2CO3 (KOAc) afforded mixtures of isomeric N-acetyl-7-methyl-3,3a,4,8b- and -1,3a,4,8b-tetrahydrocyclopenta[b]indoles at a ratio of 3: 1 or N-acetyl-5,7-dimethyl-3,3a,4,8b- and -1,3a,4,8b-tetrahydrocyclopenta[b]indoles at a ratio of 2: 3. N-Acetyl-3,3a,4,8b-tetrahydrocyclopenta[b]indole was found to undergo thermal isomerization into N-acetyl-1,3a,4,8btetrahydrocyclopenta[b] indole.

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