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183734-04-5

Benzeneacetic acid, a-(formylamino)-a-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 183734-04-5 Structure

  • Basic information

    1. Product Name: Benzeneacetic acid, a-(formylamino)-a-phenyl-
    2. Synonyms:
    3. CAS NO:183734-04-5
    4. Molecular Formula: C15H13NO3
    5. Molecular Weight: 255.273
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 183734-04-5.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: Benzeneacetic acid, a-(formylamino)-a-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzeneacetic acid, a-(formylamino)-a-phenyl-(183734-04-5)
    11. EPA Substance Registry System: Benzeneacetic acid, a-(formylamino)-a-phenyl-(183734-04-5)

  • 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: 183734-04-5(Hazardous Substances Data)

183734-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183734-04-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,7,3 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 183734-04:
(8*1)+(7*8)+(6*3)+(5*7)+(4*3)+(3*4)+(2*0)+(1*4)=145
145 % 10 = 5
So 183734-04-5 is a valid CAS Registry Number.

183734-04-5Relevant articles and documents

Synthesis of tripeptides containing α,α-diphenylglycine by the modified Ugi reaction

Yamada, Takashi,Omote, Yuichiro,Yamanaka, Yoshinori,Miyazawa, Toshifumi,Kuwata, Shigeru

, p. 991 - 998 (2007/10/03)

The modified Ugi reaction has been developed to synthesize tripeptides containing α,α-diphenylglycine (Dph) together with bulky amino acids. By the use of diphenylmethanimine, N-benzyloxycarbonyl (Z) amino acids and isocyanides derived from amino acids, very crowded tripeptides such as Z- Aib-Dph-Aib-OMe, Z-Ac6c-Dph-Aib-OMe, Z-Dph-Dph-Dph-OMe, etc. have been synthesized.

A novel modification of the Ritter reaction using trimethylsilyl cyanide

Chen,Goel,Kesten,Knobelsdorf

, p. 8129 - 8132 (2007/10/03)

A new modification of the Ritter reaction using trimethylsilyl cyanide (Me3SiCN) is described, which converts alcohols to their corresponding formamides in high yields using a convenient procedure. The reaction conditions and mechanism are discussed. In some cases, new formamides are synthesized which cannot be prepared by the classical Ritter reaction.

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