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CAS

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124920-11-2

N-(1-Dimethoxymethyl-pentyl)-4-methyl-benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124920-11-2 Structure

  • Basic information

    1. Product Name: N-(1-Dimethoxymethyl-pentyl)-4-methyl-benzenesulfonamide
    2. Synonyms: N-(1-Dimethoxymethyl-pentyl)-4-methyl-benzenesulfonamide
    3. CAS NO:124920-11-2
    4. Molecular Formula:
    5. Molecular Weight: 315.434
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124920-11-2.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: N-(1-Dimethoxymethyl-pentyl)-4-methyl-benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(1-Dimethoxymethyl-pentyl)-4-methyl-benzenesulfonamide(124920-11-2)
    11. EPA Substance Registry System: N-(1-Dimethoxymethyl-pentyl)-4-methyl-benzenesulfonamide(124920-11-2)

  • 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: 124920-11-2(Hazardous Substances Data)

124920-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124920-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,9,2 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124920-11:
(8*1)+(7*2)+(6*4)+(5*9)+(4*2)+(3*0)+(2*1)+(1*1)=102
102 % 10 = 2
So 124920-11-2 is a valid CAS Registry Number.

124920-11-2Downstream Products

124920-11-2Relevant articles and documents

Electroorganic chemistry. 120. New patterns of anodic oxidation of amides. Synthesis of α-amino aldehyde acetals and pyrrolidines from amines

Shono, Tatsuya,Matsumura, Yoshihiro,Katoh, Susumu,Takeuchi, Kei,Sasaki, Katsushi,Kamada, Tohru,Shimizu, Rie

, p. 2368 - 2372 (2007/10/02)

Anodic oxidation of N-alkyltosylamides 1 in methanol containing KX (X = Br, I) gave two types of products, α-(tosylamino) aldehyde acetals 2 and pyrrolidine derivatives 3, and each of the products could selectively be formed by modifying the reaction conditions when the alkyl group on the nitrogen of 1 was not branched at its α-position. Namely, anodic oxidation ot N-(α-unbranched alkyl)tosylamides 1a-g in methanol containing NaOMe and KI at -10°C followed by further anodic oxidation at 25°C afforded 2 in good yields, while that of 1 in a two-layer system consisting of cyclohexane and water containing KOH and KBr under heating yielded solely 3. On the other hand, N-(α-branched alkyl)tosylamides 1h-j gave always 3. Two types of reaction routes leading to each of the products were proposed.

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