Cas no 37435-12-4 (7-Chloro-1H-indazole)

7-Chloro-1H-indazole structure
7-Chloro-1H-indazole structure
Product Name:7-Chloro-1H-indazole
CAS No:37435-12-4
MF:C7H5ClN2
MW:152.581000089645
MDL:MFCD07368214
CID:54705
PubChem ID:11116249
Update Time:2025-04-18

7-Chloro-1H-indazole Chemical and Physical Properties

Names and Identifiers

    • 7-chloro-1H-indazole
    • 7-CHLOROINDAZOLE
    • 1H-Indazole, 7-chloro-
    • 7-chlor-1H-indazol
    • WIYOYUQVNPTVQG-UHFFFAOYSA-N
    • 7-Chloro-1H-indazole, AldrichCPR
    • BCP27378
    • STL554161
    • SBB054730
    • OR3680
    • FCH921470
    • BBL100367
    • BDBM50209244
    • PB17411
    • VI20076
    • BL000561
    • ST1100712
    • AB0038059
    • AX8028537
    • EN300-174788
    • SCHEMBL104360
    • AM20040313
    • FT-0648019
    • AKOS005072025
    • MFCD07368214
    • A15536
    • J-519185
    • 37435-12-4
    • CS-0044712
    • PD183094
    • DTXSID80455690
    • SY064846
    • CB-0833
    • CHEMBL247367
    • AC-14821
    • SCHEMBL19152469
    • DTXCID60406509
    • DB-026426
    • 7-Chloro-1H-indazole
    • MDL： MFCD07368214
    • Inchi： 1S/C7H5ClN2/c8-6-3-1-2-5-4-9-10-7(5)6/h1-4H,(H,9,10)
    • InChI Key： WIYOYUQVNPTVQG-UHFFFAOYSA-N
    • SMILES： ClC1=CC=CC2C=NNC=21

Computed Properties

  • Exact Mass: 152.01400
  • Monoisotopic Mass: 152.0141259g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 0
  • Complexity: 129
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 28.7
  • XLogP3: 2.2

Experimental Properties

  • Density: 1.425
  • Melting Point: 135-137
  • Boiling Point: 309.5°C at 760 mmHg
  • Flash Point: 309.536 °C at 760 mmHg
  • Refractive Index: 1.703
  • PSA: 28.68000
  • LogP: 2.21630

7-Chloro-1H-indazole Security Information

7-Chloro-1H-indazole Customs Data

  • HS CODE：2933990090
  • Customs Data：

    China Customs Code:

    2933990090

    Overview:

    2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

7-Chloro-1H-indazole Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Fluorochem
067652-1g
7-Chloro-1H-indazole
 37435-12-4 97%
1g
 ￡48.00 2022-03-01
Fluorochem
067652-5g
7-Chloro-1H-indazole
 37435-12-4 97%
5g
 ￡169.00 2022-03-01
Fluorochem
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 37435-12-4 97%
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 ￡653.00 2022-03-01
Alichem
A269001420-5g
7-Chloro-1H-indazole
 37435-12-4 95%
5g
 277.20 USD 2021-06-01
TRC
B418648-50mg
7-Chloro-1H-indazole
 37435-12-4
50mg
 $ 50.00 2022-06-07
TRC
B418648-100mg
7-Chloro-1H-indazole
 37435-12-4
100mg
 $ 65.00 2022-06-07
TRC
B418648-500mg
7-Chloro-1H-indazole
 37435-12-4
500mg
 $ 160.00 2022-06-07
CHENG DOU FEI BO YI YAO Technology Co., Ltd.
FB05577-25g
7-chloro-1H-indazole
 37435-12-4 95%
25g
 $585 2023-09-07
JIE DA WEI （ SHANG HAI ） YI YAO KE JI FA ZHAN Co., Ltd.
45R0234-1g
7-Chloro-1H-indazole
 37435-12-4 96%
1g
 466.42CNY 2021-05-08
JIE DA WEI （ SHANG HAI ） YI YAO KE JI FA ZHAN Co., Ltd.
45R0234-5g
7-Chloro-1H-indazole
 37435-12-4 96%
5g
 1441.67CNY 2021-05-08

7-Chloro-1H-indazole Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Hydrazine
Reference
2-Fluorobenzaldehyde
Lukin, Kirill, e-EROS Encyclopedia of Reagents for Organic Synthesis, 2007, ,

7-Chloro-1H-indazole Raw materials

7-Chloro-1H-indazole Preparation Products

7-Chloro-1H-indazole Related Literature

  • 1. A simple and convenient deamination of aromatic amines
    J. I. G. Cadogan,G. A. Molina J. Chem. Soc. Perkin Trans. 1 1973 541
  • 2. 185. The kinetics and mechanisms of aromatic halogen substitution. Part XII. Products of chlorination of fluorene in acetic acid
    G. H. Beaven,P. B. D. de la Mare,E. A. Johnson,N. V. Klassen J. Chem. Soc. 1962 988

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