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3-Iodophenylacetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1878-69-9 Structure
  • Basic information

    1. Product Name: 3-Iodophenylacetic acid
    2. Synonyms: 3-IODOPHENYLACETIC ACID;RARECHEM AL BO 0414;M-IODOPHENYLACETIC ACID;m-Iodobenzeneacetic acid;2-(3-iodophenyl)acetic acid;3-Iodobenzeneacetic acid
    3. CAS NO:1878-69-9
    4. Molecular Formula: C8H7IO2
    5. Molecular Weight: 262.04
    6. EINECS: -0
    7. Product Categories: Aromatic Phenylacetic Acids and Derivatives;Phenylacetic acid;C8;Carbonyl Compounds;Carboxylic Acids;Building Blocks;Carbonyl Compounds;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks
    8. Mol File: 1878-69-9.mol
  • Chemical Properties

    1. Melting Point: 127-131 °C(lit.)
    2. Boiling Point: 347.2°Cat760mmHg
    3. Flash Point: 163.8°C
    4. Appearance: /
    5. Density: 1.885g/cm3
    6. Vapor Pressure: 2.07E-05mmHg at 25°C
    7. Refractive Index: 1.643
    8. Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: pK1:4.159 (25°C)
    11. Sensitive: Light Sensitive
    12. BRN: 2501867
    13. CAS DataBase Reference: 3-Iodophenylacetic acid(CAS DataBase Reference)
    14. NIST Chemistry Reference: 3-Iodophenylacetic acid(1878-69-9)
    15. EPA Substance Registry System: 3-Iodophenylacetic acid(1878-69-9)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: IRRITANT, LIGHT SENSITIVE
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1878-69-9(Hazardous Substances Data)

1878-69-9 Usage

Chemical Properties

White to light yellow solid

Check Digit Verification of cas no

The CAS Registry Mumber 1878-69-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,7 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1878-69:
(6*1)+(5*8)+(4*7)+(3*8)+(2*6)+(1*9)=119
119 % 10 = 9
So 1878-69-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H7IO2/c9-7-3-1-2-6(4-7)5-8(10)11/h1-4H,5H2,(H,10,11)

1878-69-9 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (L15117)  3-Iodophenylacetic acid, 98%   

  • 1878-69-9

  • 500mg

  • 370.0CNY

  • Detail
  • Alfa Aesar

  • (L15117)  3-Iodophenylacetic acid, 98%   

  • 1878-69-9

  • 2g

  • 1181.0CNY

  • Detail

1878-69-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-iodophenyl)acetic acid

1.2 Other means of identification

Product number -
Other names 3-Iodophenylacetic Acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1878-69-9 SDS

1878-69-9Relevant articles and documents

Specific targeting highly conserved residues in the HIV-1 reverse transcriptase primer grip region. Design, synthesis, and biological evaluation of novel, potent, and broad spectrum NNRTIs with antiviral activity

Fattorusso, Caterina,Gemma, Sandra,Butini, Stefania,Huleatt, Paul,Catalanotti, Bruno,Persico, Marco,De Angelis, Meri,Fiorini, Isabella,Nacci, Vito,Ramunno, Anna,Rodriquez, Manuela,Greco, Giovanni,Novellino, Ettore,Bergamini, Alberto,Marini, Stefano,Coletta, Massimo,Maga, Giovanni,Spadari, Silvio,Campiani, Giuseppe

, p. 7153 - 7165 (2007/10/03)

Pyrrolobenzoxazepinones (PBOs) represent a new class of human immunodeficiency virus type 1 (HIV-1) nonnucleoside reverse transcriptase (RT) inhibitors (NNRTIs) whose prototype is 5. Molecular modeling studies based on the X-ray structures of HIV-1 RT pro

Novel thiophene derivatives, their process of preparation and the pharmaceutical compositions which comprise them

-

Page/Page column 19, (2010/11/30)

A compound of formula (I) selected from: wherein: X represents oxygen or sulphur, Y represents oxygen, —NH— or —N(C1-C6)alkyl-, Ra represents hydrogen, halogen, (C1-C3)alkyl, hydroxyl or (C1-C3)alkoxy, Rb represents hydrogen, halogen or (C1-C3)alkyl, A represents phenyl, pyridyl, (C5-C6)cycloalkyl or (C5-C6)cycloalkenyl, R1 and R2 each represent a group selected from hydrogen, halogen, cyano, nitro, haloalkyl, haloalkoxy, alkyl, alkenyl, alkynyl, —OR4, —NR4R5, —S(O)nR4, —C(O)R4, —CO2R4, —O—C(O)R4, —C(O)NR4R5, —NR5—C(O)R4, —NR5—SO2R4, -T-CN, -T-OR4, -T-OCF3, -T- NR4R5, -T-S(O)nR4, -T-C(O)R4, -T-CO2R4, -T-O—C(O)R4, -T-C(O)NR4R5, -T-NR4—C(O)R5, -T-NR4—SO2R5, —R6 and -T-R6 in which n, T, R4, R5 and R6 are as defined in the description, R3 represents an —R7 or —U—R11 group in which R7 represents hydrogen, alkyl, aryl, cycloalkyl or heterocycle, U represents a linear or branched alkylene chain and R11 is defined in the description, their optical isomers or their addition salts with a pharmaceutically acceptable acid or base, and their use as inhibitor of metalloproteinase and more specifically of metalloproteinase-12.

Synthesis of phenylacetic acids under rhodium-catalyzed carbonylation conditions

Giroux,Nadeau,Han

, p. 7601 - 7604 (2007/10/03)

Benzyl halides are efficiently carbonylated to phenylacetic acids in the presence of a catalytic amount of the dimer of chloro(1,5-cyclooctadiene)rhodium(I) in formic acid. Under these reaction conditions, sensitive functionalities such as esters and nitriles are tolerated and the phenylacetic acids are obtained in good to high yields. (C) 2000 Elsevier Science Ltd.

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