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118617-57-5

N-<(o-methoxyphenylthio)methyl>formamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 118617-57-5 Structure

  • Basic information

    1. Product Name: N-<(o-methoxyphenylthio)methyl>formamide
    2. Synonyms: N-<(o-methoxyphenylthio)methyl>formamide
    3. CAS NO:118617-57-5
    4. Molecular Formula:
    5. Molecular Weight: 197.258
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 118617-57-5.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-<(o-methoxyphenylthio)methyl>formamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-<(o-methoxyphenylthio)methyl>formamide(118617-57-5)
    11. EPA Substance Registry System: N-<(o-methoxyphenylthio)methyl>formamide(118617-57-5)

  • 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: 118617-57-5(Hazardous Substances Data)

118617-57-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118617-57-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,6,1 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 118617-57:
(8*1)+(7*1)+(6*8)+(5*6)+(4*1)+(3*7)+(2*5)+(1*7)=135
135 % 10 = 5
So 118617-57-5 is a valid CAS Registry Number.

118617-57-5Relevant articles and documents

Asmic: An Exceptional Building Block for Isocyanide Alkylations

Alwedi, Embarek,Lujan-Montelongo, J. Armando,Pitta, Bhaskar R.,Chao, Allen,Cortés-Mejía, Rodrigo,Del Campo, Jorge M.,Fleming, Fraser F.

, p. 5910 - 5913 (2018)

Asmic addresses the long-standing challenge of alkylating isocyanides, providing access to isocyanides with diverse substitution patterns. The o-anisylsulfanyl group serves a critical dual role by facilitating deprotonation-alkylation and providing a latent nucleophilic site through an unusual arylsulfanyl-lithium exchange.

COMPOSITION, SYNTHESIS, AND USE OF A NEW CLASS OF ISONITRILES

-

Paragraph 0050, (2015/09/23)

This invention relates to novel isonitriles, including arylthio isonitriles, and methods for their preparation. The isonitriles include a conjugated ring system. The structure is designed with the flexibility to have multiple substitution patterns. The isonitriles may be used in applications including, but not limited to, pharmaceutical compositions.

SYNTHESIS OF CHIRAL SULFONYLMETHYL ISOCYANIDES, AND COMPARISON OF THEIR PROPENSITIES IN ASYMMETRIC INDUCTION REACTIONS WITH ACETOPHENONES

Hundscheid, Frans J. A.,Tandon, Vishnu K.,Rouwette, Pieter H. F. M.,Leusen, Albert M. van

, p. 5073 - 5088 (2007/10/02)

Seven chiral analogues of tosylmethyl isocyanide (TosMIC) were synthesized in order to investigate and compare their ability to achieve asymmetric induction in base mediated reactions with acetophenone and trifluoracetophenone.Acid hydrolysis of the intermediate 2-oxazolines (10 and 11) gave optically active α-hydroxy aldehydes (12 and 13).

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