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4-methyl-N-(octa-6,7-dien-1-yl)benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132927-86-7 Structure
  • Basic information

    1. Product Name: 4-methyl-N-(octa-6,7-dien-1-yl)benzenesulfonamide
    2. Synonyms: 4-methyl-N-(octa-6,7-dien-1-yl)benzenesulfonamide
    3. CAS NO:132927-86-7
    4. Molecular Formula:
    5. Molecular Weight: 279.403
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132927-86-7.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: 4-methyl-N-(octa-6,7-dien-1-yl)benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-methyl-N-(octa-6,7-dien-1-yl)benzenesulfonamide(132927-86-7)
    11. EPA Substance Registry System: 4-methyl-N-(octa-6,7-dien-1-yl)benzenesulfonamide(132927-86-7)
  • 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: 132927-86-7(Hazardous Substances Data)

132927-86-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132927-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,9,2 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132927-86:
(8*1)+(7*3)+(6*2)+(5*9)+(4*2)+(3*7)+(2*8)+(1*6)=137
137 % 10 = 7
So 132927-86-7 is a valid CAS Registry Number.

132927-86-7Relevant articles and documents

Medium and Large N-Heterocycle Formation via Allene Hydroamination with a Bimetallic Rh(II) Catalyst

Bohman, Benjamin O.,Davis, Rhen C.,Forson, Kelton G.,McKnight, Caitlyn E.,Michaelis, David J.,Owens, Rachel N.,Smith, Stacey J.,Stillwell, Lillian R.,Wayment, Coriantumr Z.

, p. 63 - 68 (2022/01/19)

We report the synthesis of a 2-phosphinoimidazole-derived bimetallic Rh(II) complex that enables intramolecular allene hydroamination to form 7- to 10-member rings in high yield. Monometallic Rh complexes, in contrast, fail to achieve any product formatio

Allene-based Electrophile-mediated Cyclisations: Efficient Synthesis of Medium Ring Azacycles

Shaw, Robert W.,Gallagher, Timothy

, p. 3549 - 3556 (2007/10/02)

While AgI- and PdII-based electrophiles have limited application in cyclisation of allenic amines leading to 7-membered and larger azacycles, these rings may be obtained using iodine as the electrophilic trigger.Iodination of the N-b

Electrophile-mediated Cyclisations involving the Allene ?-System. Stereoselectivity and Synthetic Utility of PdII-Catalysed Heteroatom Cyclisation Reactions. X-Ray Molecular Structure of Methyl 2-

Gallagher, Timothy,Davies, Ian W.,Jones, Stephen W.,Lathbury, David,Mahon, Mary F.,et al.

, p. 433 - 440 (2007/10/02)

PdII-mediated cyclisation and methoxycarbonylation of the phenyl-substituted allenic sulfonamides 4, 5 and 6 gave the corresponding N-sulfonyl 2,3-, 2,4- and 2,5-disubstituted pyrrolidines 9, 10 and 11, respectively.With the exception of compou

Application of Electrophile-mediated Cyclisations to the Synthesis of the Hexahydroazepine Ring System

Shaw, Robert,Lathbury, David,Anderson, Martin,Gallagher, Timothy

, p. 659 - 660 (2007/10/02)

Allenic oxime 6 undergoes efficient AgI-catalysed cyclisation to give the hexahydroazepine-based nitrone 7; this reactive 1,3-dipole was subsequently trapped by styrene and N-methylmaleimide to give the adducts 8 and 9 respectively.

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