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1-azido-3-(azidomethyl)-5-iodobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1157852-35-1 Structure
  • Basic information

    1. Product Name: 1-azido-3-(azidomethyl)-5-iodobenzene
    2. Synonyms: 1-azido-3-(azidomethyl)-5-iodobenzene
    3. CAS NO:1157852-35-1
    4. Molecular Formula:
    5. Molecular Weight: 300.061
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1157852-35-1.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: 1-azido-3-(azidomethyl)-5-iodobenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-azido-3-(azidomethyl)-5-iodobenzene(1157852-35-1)
    11. EPA Substance Registry System: 1-azido-3-(azidomethyl)-5-iodobenzene(1157852-35-1)
  • 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: 1157852-35-1(Hazardous Substances Data)

1157852-35-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1157852-35-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,7,8,5 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1157852-35:
(9*1)+(8*1)+(7*5)+(6*7)+(5*8)+(4*5)+(3*2)+(2*3)+(1*5)=171
171 % 10 = 1
So 1157852-35-1 is a valid CAS Registry Number.

1157852-35-1Relevant articles and documents

Synthesis of diverse 3-azido-5-(azidomethyl)benzene derivatives via formal C-H azidation and functional group-selective transformations

Nishiyama, Yoshitake,Misawa, Yoshihiro,Hazama, Yuki,Oya, Kazuhiro,Yoshida, Suguru,Hosoya, Takamitsu

, p. 1053 - 1072 (2019/07/31)

3-Azido-5-(azidomethyl)benzene derivatives are useful compounds for preparing diverse bistriazole compounds and photoaffinity probes for target identification of bioactive compounds. To more easily synthesize a diverse range of diazido compounds, a facile

Formal C-H-azidation-based shortcut to diazido building blocks for the versatile preparation of photoaffinity labeling probes

Yoshida, Suguru,Misawa, Yoshihiro,Hosoya, Takamitsu

, p. 3991 - 3995 (2014/07/08)

Short synthetic routes to diazido building blocks with different connectable groups were established on the basis of the sequential iridium-catalyzed C-H borylation and copper-catalyzed azidation of 1,3-disubstituted benzenes, followed by diverse azido-fr

Facile synthesis of diazido-functionalized biaryl compounds as radioisotope-free photoaffinity probes by Suzuki-Miyaura coupling

Hosoya, Takamitsu,Inoue, Atsushi,Hiramatsu, Toshiyuki,Aoyama, Hiroshi,Ikemoto, Takaaki,Suzuki, Masaaki

experimental part, p. 2490 - 2496 (2009/09/25)

Suzuki-Miyaura coupling of 3-azido-5-(azidomethyl)phenylboronic acid pinacol ester with various aryl bromides affords corresponding diazido-functionalized biaryl compounds in good yields. This approach provides an easy access to radioisotope-free photoaff

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