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2,3-dihydro-1H-perimidine-2,2-diyldimethanol is a chemical compound characterized by its molecular formula C11H14N2O2. It features a perimidine ring structure and is classified as a diol compound. This versatile molecule is widely recognized for its utility as a building block in organic synthesis, underpinning its value in pharmaceutical research and development, material science for novel polymer synthesis, and as a reagent in chemical reactions for the formation of a variety of organic compounds. Furthermore, it has garnered interest for its potential biological activities and medical implications, showcasing its multifaceted role in the scientific and industrial domains.

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  • 176180-03-3 Structure
  • Basic information

    1. Product Name: 2,3-dihydro-1H-perimidine-2,2-diyldimethanol
    2. Synonyms: 1H-perimidine-2,2(3H)-dimethanol; 2,3-Dihydro-1H-perimidine-2,2-diyldimethanol
    3. CAS NO:176180-03-3
    4. Molecular Formula: C13H14N2O2
    5. Molecular Weight: 230.2625
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 176180-03-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 533.8°C at 760 mmHg
    3. Flash Point: 254.3°C
    4. Appearance: N/A
    5. Density: 1.277g/cm3
    6. Vapor Pressure: 3.17E-12mmHg at 25°C
    7. Refractive Index: 1.654
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,3-dihydro-1H-perimidine-2,2-diyldimethanol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,3-dihydro-1H-perimidine-2,2-diyldimethanol(176180-03-3)
    12. EPA Substance Registry System: 2,3-dihydro-1H-perimidine-2,2-diyldimethanol(176180-03-3)
  • 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: 176180-03-3(Hazardous Substances Data)

176180-03-3 Usage

Uses

Used in Pharmaceutical Research and Development:
2,3-dihydro-1H-perimidine-2,2-diyldimethanol serves as a crucial building block in the synthesis of pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents. Its unique chemical structure allows for the creation of diverse molecular entities with potential medicinal properties.
Used in Material Science:
In the field of material science, 2,3-dihydro-1H-perimidine-2,2-diyldimethanol is utilized for the synthesis of innovative polymers. Its incorporation into polymeric materials can enhance their properties, such as stability, reactivity, or biocompatibility, depending on the specific application.
Used as a Reagent in Chemical Reactions:
2,3-dihydro-1H-perimidine-2,2-diyldimethanol acts as a reagent in various chemical reactions, facilitating the formation of a broad spectrum of organic compounds. Its role in these reactions is pivotal for the advancement of organic chemistry and the synthesis of complex molecules.
Used in Biological Research:
2,3-dihydro-1H-perimidine-2,2-diyldimethanol has been the subject of studies exploring its potential biological activities. Its interaction with biological systems offers insights into possible medical applications, making it a valuable tool in biological and medical research.
Overall, 2,3-dihydro-1H-perimidine-2,2-diyldimethanol is a multifunctional chemical entity with applications spanning across pharmaceuticals, materials science, chemical synthesis, and biological research, highlighting its significance in the scientific and industrial landscape.

Check Digit Verification of cas no

The CAS Registry Mumber 176180-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,1,8 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 176180-03:
(8*1)+(7*7)+(6*6)+(5*1)+(4*8)+(3*0)+(2*0)+(1*3)=133
133 % 10 = 3
So 176180-03-3 is a valid CAS Registry Number.

176180-03-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(hydroxymethyl)-1,3-dihydroperimidin-2-yl]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:176180-03-3 SDS

176180-03-3Downstream Products

176180-03-3Relevant articles and documents

Solvent- and catalyst-free synthesis of 2,3-dihydro-1H-benzo[d]imidazoles

Li, Da-Peng,Zhang, Guang-Liang,An, Li-Tao,Zou, Jian-Ping,Zhang, Wei

supporting information; experimental part, p. 594 - 597 (2011/05/06)

Reactions of acyclic ketones and o-phenylenediamines under solvent- and catalyst-free conditions have been developed for the preparation of dihydrobenzimidazoles. This method can also be used for the synthesis of other heterocyclic compounds such as dihydrobenzothiazoles and perimidines. The Royal Society of Chemistry.

Method of making dihydroperimidine squaraine compounds

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Page column 15, (2010/11/29)

A method to make squaraine dyes involves the reaction of 1,8-diaminonaphthalene with 1,3-dihydroxyacetone dimer in a first reaction mixture comprising the appropriate solvents to prepare a first intermediate. This first intermediate is then reacted with a

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