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(1-(5-bromopyridin-3-yl)cyclopropyl)methanol is a cyclopropyl alcohol derivative featuring a bromopyridine substituent. This colorless, crystalline solid is utilized in laboratory and chemical research settings.
Used in Pharmaceutical Industry:
(1-(5-bromopyridin-3-yl)cyclopropyl)methanol is used as an intermediate in the synthesis of various organic compounds, particularly for the development of pharmaceuticals. Its cyclopropyl group serves as a valuable building block, contributing to the creation of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, (1-(5-bromopyridin-3-yl)cyclopropyl)methanol is also utilized as an intermediate in the synthesis of various organic compounds, playing a role in the development of agrochemicals to improve crop protection and yield.
Used in Synthetic Chemistry:
(1-(5-bromopyridin-3-yl)cyclopropyl)methanol is employed as a versatile chemical in synthetic chemistry due to its unique structure and properties, which facilitate its use in the creation of a wide range of chemical compounds.
Used in Drug Discovery:
(1-(5-broMopyridin-3-yl)cyclopropyl)Methanol is used in drug discovery efforts for its potential to contribute to the development of new pharmaceuticals, given its role as a synthetic intermediate and its compatibility with various chemical reactions.

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  • 1369503-74-1 Structure
  • Basic information

    1. Product Name: (1-(5-broMopyridin-3-yl)cyclopropyl)Methanol
    2. Synonyms: (1-(5-broMopyridin-3-yl)cyclopropyl)Methanol
    3. CAS NO:1369503-74-1
    4. Molecular Formula: C9H10BrNO
    5. Molecular Weight: 228.0858
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1369503-74-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 321.8±27.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.585±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 15.10±0.10(Predicted)
    10. CAS DataBase Reference: (1-(5-broMopyridin-3-yl)cyclopropyl)Methanol(CAS DataBase Reference)
    11. NIST Chemistry Reference: (1-(5-broMopyridin-3-yl)cyclopropyl)Methanol(1369503-74-1)
    12. EPA Substance Registry System: (1-(5-broMopyridin-3-yl)cyclopropyl)Methanol(1369503-74-1)
  • 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: 1369503-74-1(Hazardous Substances Data)

1369503-74-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1369503-74-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,9,5,0 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1369503-74:
(9*1)+(8*3)+(7*6)+(6*9)+(5*5)+(4*0)+(3*3)+(2*7)+(1*4)=181
181 % 10 = 1
So 1369503-74-1 is a valid CAS Registry Number.

1369503-74-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [1-(5-bromo-3-pyridinyl)cyclopropyl]methanol

1.2 Other means of identification

Product number -
Other names -

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:1369503-74-1 SDS

1369503-74-1Downstream Products

1369503-74-1Relevant articles and documents

ALDOSTERONE SYNTHASE INHIBITORS

-

Page/Page column 104, (2012/11/13)

This invention relates to tricyclic triazole analogues of the formula I or their pharmaceutically acceptable salts, wherein the variable are defined herein. The inventive compounds selectively inhibit aldosterone synthetase. This invention also provides for pharmaceutical compositions comprising the compounds of Formula I or their salts as well as to methods for the treatment, amelioration or prevention of conditions that could be treated by inhibiting aldosterone synthetase.

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