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Benzenemethanol, 4-azido-3-iodo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 167868-43-1 Structure
  • Basic information

    1. Product Name: Benzenemethanol, 4-azido-3-iodo-
    2. Synonyms:
    3. CAS NO:167868-43-1
    4. Molecular Formula: C7H6IN3O
    5. Molecular Weight: 275.049
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 167868-43-1.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: Benzenemethanol, 4-azido-3-iodo-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenemethanol, 4-azido-3-iodo-(167868-43-1)
    11. EPA Substance Registry System: Benzenemethanol, 4-azido-3-iodo-(167868-43-1)
  • 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: 167868-43-1(Hazardous Substances Data)

167868-43-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 167868-43-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,8,6 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 167868-43:
(8*1)+(7*6)+(6*7)+(5*8)+(4*6)+(3*8)+(2*4)+(1*3)=191
191 % 10 = 1
So 167868-43-1 is a valid CAS Registry Number.

167868-43-1Relevant articles and documents

Design, synthesis, and in vitro pharmacology of new radiolabeled γ-hydroxybutyric acid analogues including photolabile analogues with irreversible binding to the high-affinity γ-hydroxybutyric acid binding sites

Sabbatini, Paola,Wellendorph, Petrine,H?g, Signe,Pedersen, Martin H. F.,Br?uner-Osborne, Hans,Martiny, Lars,Fr?lund, Bente,Clausen, Rasmus P.

supporting information; experimental part, p. 6506 - 6510 (2010/11/18)

γ-Hydroxybutyric acid (GHB) is a psychotropic compound endogenous to the brain. Despite its potential physiological significance, the complete molecular mechanisms of action remain unexplained. To facilitate the isolation and identification of the high-affinity GHB binding site, we herein report the design and synthesis of the first 125I-labeled radioligands in the field, one of which contains a photoaffinity label which enables it to bind irreversibly to the high-affinity GHB binding sites.

Synthesis of I-125 labeled photoaffinity rapamycin analogs

Shu, Arthur Y.L.,Yamashita, Dennis S.,Holt, Dennis A.,Heys, J. Richard

, p. 227 - 237 (2007/10/03)

Two no-carrier-added 125I-labeled photoaffinity rapamycin analogs were prepared: 7-demethoxy-7-(4-azido-3-125I-benzyloxy)rapamycin (2) and its C28-C29 seco analog 3. The key reactions of the synthesis were subst

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