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1310377-56-0

methyl 2-(bromomethyl)-5-iodobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1310377-56-0 Structure

  • Basic information

    1. Product Name: methyl 2-(bromomethyl)-5-iodobenzoate
    2. Synonyms:
    3. CAS NO:1310377-56-0
    4. Molecular Formula:
    5. Molecular Weight: 354.97
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1310377-56-0.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: methyl 2-(bromomethyl)-5-iodobenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-(bromomethyl)-5-iodobenzoate(1310377-56-0)
    11. EPA Substance Registry System: methyl 2-(bromomethyl)-5-iodobenzoate(1310377-56-0)

  • 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: 1310377-56-0(Hazardous Substances Data)

1310377-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1310377-56-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,3,7 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1310377-56:
(9*1)+(8*3)+(7*1)+(6*0)+(5*3)+(4*7)+(3*7)+(2*5)+(1*6)=120
120 % 10 = 0
So 1310377-56-0 is a valid CAS Registry Number.

1310377-56-0Downstream Products

1310377-56-0Relevant articles and documents

Synthesis of Conformationally-Constrained Glutamate Analogues of the Antitumor Agents DDATHF, LY254155, and LY231514

Taylor, Edward C.,Jennings, Lee D.,Mao, Zhenmin,Hu, Baihua,Jun, Jong-Gab,Zhou, Ping

, p. 5392 - 5403 (2007/10/03)

Analogues of the active antitumor agents DDATHF (4), LY254155 (11), and LY231514 (14) have been prepared in which the rotational flexibility of the benzoylglutamate amide linkage is constrained by incorporation of a methylene bridge between the glutamate amide nitrogen and the ortho position of the aromatic ring. Evaluation of the resulting isoindolinones as in vitro inhibitors of the growth of CCRF-CEM cells revealed that, although some analogues retained activity, in no case was cytotoxicity enhanced, and in some cases it was substantially reduced.

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