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80304-48-9

CHEMBRDG-BB 4016576 is a chemical compound with a unique molecular structure and chemical properties. Its exact composition and intended use are not explicitly clear, but it is likely a derivative of a specific class of compounds. Given its CHEMBRDG-BB designation, it is likely a potential lead compound for drug development or an experimental compound for research purposes.
Usage:
Since the provided materials do not specify any particular applications for CHEMBRDG-BB 4016576, it is not possible to list its uses according to the materials. Further information on its specific attributes, potential applications, and safety profile would be necessary to fully understand its relevance and potential utility in the field of chemistry and pharmaceuticals.

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  • 80304-48-9 Structure

  • Basic information

    1. Product Name: CHEMBRDG-BB 4016576
    2. Synonyms: CHEMBRDG-BB 4016576;(1-CYCLOHEXYL-1H-IMIDAZOL-5-YL)METHANOL;(1-cyclohexyl-1H-imidazol-5-yl)methanol(SALTDATA: FREE)
    3. CAS NO:80304-48-9
    4. Molecular Formula: C10H16N2O
    5. Molecular Weight: 180.25
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 80304-48-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 395.6°C at 760 mmHg
    3. Flash Point: 193°C
    4. Appearance: /
    5. Density: 1.2g/cm3
    6. Vapor Pressure: 5.73E-07mmHg at 25°C
    7. Refractive Index: 1.604
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 14.32±0.10(Predicted)
    11. CAS DataBase Reference: CHEMBRDG-BB 4016576(CAS DataBase Reference)
    12. NIST Chemistry Reference: CHEMBRDG-BB 4016576(80304-48-9)
    13. EPA Substance Registry System: CHEMBRDG-BB 4016576(80304-48-9)

  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 80304-48-9(Hazardous Substances Data)

80304-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80304-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,0 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80304-48:
(7*8)+(6*0)+(5*3)+(4*0)+(3*4)+(2*4)+(1*8)=99
99 % 10 = 9
So 80304-48-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H16N2O/c13-7-10-6-11-8-12(10)9-4-2-1-3-5-9/h6,8-9,13H,1-5,7H2

80304-48-9 Well-known Company Product Price

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  • Aldrich

  • (CBR00479)  (1-Cyclohexyl-1H-imidazol-5-yl)methanol  AldrichCPR

  • 80304-48-9

  • CBR00479-1G

  • 1,611.09CNY

  • Detail

80304-48-9SDS

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 (3-cyclohexylimidazol-4-yl)methanol

1.2 Other means of identification

Product number -
Other names 1-cyclohexyl-5-hydroxymethylimidazole

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:80304-48-9 SDS

80304-48-9Downstream Products

80304-48-9Relevant articles and documents

A Series of 2-((1-Phenyl-1H-imidazol-5-yl)methyl)-1H-indoles as Indoleamine 2,3-Dioxygenase 1 (IDO1) Inhibitors

Zheng, Yong,Stafford, Paul M.,Stover, Kurt R.,Mohan, Darapaneni Chandra,Gupta, Mayuri,Keske, Eric C.,Schiavini, Paolo,Villar, Laura,Wu, Fan,Kreft, Alexander,Thomas, Kiersten,Raaphorst, Elana,Pasangulapati, Jagadeesh P.,Alla, Siva R.,Sharma, Simmi,Mittapalli, Ramana R.,Sagamanova, Irina,Johnson, Shea L.,Reed, Mark A.,Weaver, Donald F.

supporting information, p. 2195 - 2205 (2021/05/31)

Indoleamine 2,3-dioxygenase 1 (IDO1) is a promising therapeutic target in cancer immunotherapy and neurological disease. Thus, searching for highly active inhibitors for use in human cancers is now a focus of widespread research and development efforts. I

Process for the production of hydroxymethylimidazoles

-

, (2008/06/13)

This invention discloses a process for the production of hydroxymethylimidazoles which comprises reacting imidazolecarboxylic acids, their esters or inorganic salts with a formaldehyde agent in the presence of an alkali in an aqueous medium.

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