133841-05-1

• 

• Basic information

  1. Product Name: 7-METHOXY-1H-INDAZOLE
  2. Synonyms: 7-METHOXY-1H-INDAZOLE;1H-Indazole, 7-methoxy-
  3. CAS NO:133841-05-1
  4. Molecular Formula: C₈H₈N₂O
  5. Molecular Weight: 148.16192
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 133841-05-1.mol
  9. Article Data: 7

• Chemical Properties

  1. Melting Point: 91-92 °C
  2. Boiling Point: 312.5 °C at 760 mmHg
  3. Flash Point: 114.6 °C
  4. Appearance: /
  5. Density: 1.244 g/cm³
  6. Vapor Pressure: 0.000968mmHg at 25°C
  7. Refractive Index: 1.647
  8. Storage Temp.: Sealed in dry,Room Temperature
  9. Solubility: N/A
  10. PKA: 13.33±0.40(Predicted)
  11. CAS DataBase Reference: 7-METHOXY-1H-INDAZOLE(CAS DataBase Reference)
  12. NIST Chemistry Reference: 7-METHOXY-1H-INDAZOLE(133841-05-1)
  13. EPA Substance Registry System: 7-METHOXY-1H-INDAZOLE(133841-05-1)

• 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: 133841-05-1(Hazardous Substances Data)

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• Downstream Products
• Article

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• 7-Methoxy-1H-Indazole

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• (2-ISOPROPOXY-PYRIDIN-3-YL)-METHANOL

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133841-05-1 Usage

Uses

7-Methoxy-1H-indazole is an inhibitor of neuronal nitric oxide synthase.

Check Digit Verification of cas no

The CAS Registry Mumber 133841-05-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,8,4 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 133841-05:
(8*1)+(7*3)+(6*3)+(5*8)+(4*4)+(3*1)+(2*0)+(1*5)=111
111 % 10 = 1
So 133841-05-1 is a valid CAS Registry Number.

InChI:InChI=1/C8H8N2O/c1-11-7-4-2-3-6-5-9-10-8(6)7/h2-5H,1H3,(H,9,10)

133841-05-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	7-Methoxy-1H-indazole

1.2 Other means of identification

Product number	-
Other names	7-methoxy-1H-indazole

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:133841-05-1 SDS

133841-05-1Upstream product

• 64420-86-6 O-p-toluenesulfonyl benzyloxyhydroxamate 
• 54881-49-1 2-chloro-3-methoxy benzaldehyde 
• 77774-35-7 N-(2-hydroxy-6-methylphenyl)acetamide 
• 2835-97-4 2-amino-3-methylphenol 
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• 321-28-8 1-fluoro-2-methoxybenzene 
• 409321-32-0 C₈H₁₀N₂O₂ 
• 50868-76-3 N-(2-methoxy-6-methylphenyl)acetamide 

133841-05-1Downstream Products

• 351210-09-8 7-benzyloxyindazole 
• 351210-07-6 3-iodo-7-methoxy-1H-indazole 
• 81382-46-9 7-hydroxy-1H-indazole 

133841-05-1Relevant articles and documents

Facile synthesis of 3-trimethylsilylindazoles by [3+2]cycloaddition reaction of lithium trimethylsilyldiazomethane with benzynes

Shoji, Yoshimichi,Hari, Yoshiyuki,Aoyama, Toyohiko

, p. 1769 - 1771 (2004)

[3+2]Cycloaddition reaction of lithium trimethylsilyldiazomethane with benzynes, generated from halobenzenes, gave the corresponding 3-trimethylsilylindazoles in good to moderate yields.

NOVEL CATALYSTS

-

Page/Page column 60, (2012/06/01)

The present invention provides novel compounds and ligands that are useful in transition metal catalyzed cross-coupling reactions. For example, the compounds and ligands of the present invention are useful in palladium or gold catalyzed cross-coupling reactions.

Toward biophysical probes for the 5-HT3 receptor: Structure-activity relationship study of granisetron derivatives

Vernekar, Sanjeev Kumar V.,Hallaq, Hasan Y.,Clarkson, Guy,Thompson, Andrew J.,Silvestr, Linda,Lummis, Sarah C. R.,Lochner, Martin

supporting information; experimental part, p. 2324 - 2328 (2010/07/17)

This report describes the synthesis and biological characterization of novel granisetron derivatives that are antagonists of the human serotonin (5-HT3A) receptor. Some of these substituted granisetron derivatives showed low nanomolar binding affinity and allowed the identification of positions on the granisetron core that might be used as attachment points for biophysical tags. A BODIPY fluorophore was appended to one such position and specifically bound to 5-HT3A receptors in mammalian cells.

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