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(2,5-DIMETHYL-1,3-OXAZOL-4-YL)METHANOL is a chemical compound that belongs to the class of organic compounds known as oxazoles. It is characterized by an oxazol ring, which is a five-membered aromatic ring containing an oxygen atom and a nitrogen atom. The specific structure of this compound includes a 1,3-oxazol-4-yl methanol with two methyl substituents at the 2 and 5 positions of the oxazole ring. Its molecular formula indicates the presence of carbon, hydrogen, nitrogen, and oxygen atoms. However, due to its less common occurrence in commercial or industrial settings, the uses and potential hazards of this compound may not be extensively reviewed or detailed. (2,5-DIMETHYL-1,3-OXAZOL-4-YL)METHANOL's potential toxicity and other physical and chemical properties necessitate a thorough investigation of its exposure effects, and it should be handled with care and appropriate protective measures.

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  • 92901-94-5 Structure
  • Basic information

    1. Product Name: (2,5-DIMETHYL-1,3-OXAZOL-4-YL)METHANOL
    2. Synonyms: (2,5-DIMETHYL-1,3-OXAZOL-4-YL)METHANOL;(2,5-Dimethyl-1,3-oxazol-4-yl)methanol 97%;2,5-Dimethyl-4-(hydroxymethyl)-1,3-oxazole;(2,5-Dimethyloxazol-4-yl)methanol;2,5-Dimethyl-4-(hydroxymethyl)-1,3-oxazole 97%;2,5-Dimethyl-4-(hydroxymethyl)-1,3-oxazole97%
    3. CAS NO:92901-94-5
    4. Molecular Formula: C6H9NO2
    5. Molecular Weight: 127.14
    6. EINECS: 200-258-5
    7. Product Categories: N/A
    8. Mol File: 92901-94-5.mol
  • Chemical Properties

    1. Melting Point: 73 °C
    2. Boiling Point: 222.012 °C at 760 mmHg
    3. Flash Point: 88.07 °C
    4. Appearance: /
    5. Density: 1.137 g/cm3
    6. Vapor Pressure: 0.06mmHg at 25°C
    7. Refractive Index: 1.497
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. PKA: 13.15±0.10(Predicted)
    11. CAS DataBase Reference: (2,5-DIMETHYL-1,3-OXAZOL-4-YL)METHANOL(CAS DataBase Reference)
    12. NIST Chemistry Reference: (2,5-DIMETHYL-1,3-OXAZOL-4-YL)METHANOL(92901-94-5)
    13. EPA Substance Registry System: (2,5-DIMETHYL-1,3-OXAZOL-4-YL)METHANOL(92901-94-5)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36
    3. Safety Statements: 26
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 92901-94-5(Hazardous Substances Data)

92901-94-5 Usage

Uses

Given the provided materials, there are no specific applications or uses mentioned for (2,5-DIMETHYL-1,3-OXAZOL-4-YL)METHANOL. However, based on its chemical structure and belonging to the class of oxazoles, it may have potential applications in various industries, such as pharmaceuticals, materials science, or chemical research. Further investigation and research would be required to explore and confirm its potential uses and benefits in these or other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 92901-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,0 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92901-94:
(7*9)+(6*2)+(5*9)+(4*0)+(3*1)+(2*9)+(1*4)=145
145 % 10 = 5
So 92901-94-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO2/c1-4-6(3-8)7-5(2)9-4/h8H,3H2,1-2H3

92901-94-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,5-Dimethyloxazol-4-yl)methanol

1.2 Other means of identification

Product number -
Other names (2,5-DIMETHYL-1,3-OXAZOL-4-YL)METHANOL

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:92901-94-5 SDS

92901-94-5Relevant articles and documents

Synthesis and evaluation of a novel series of 2,7-substituted-6-tetrazolyl-1,2,3,4-tetrahydroisoquinoline derivatives as selective peroxisome proliferator-activated receptor γ partial agonists

Morishita, Ko,Ito, Yuma,Otake, Kazuya,Takahashi, Kenji,Yamamoto, Megumi,Kitao, Tatsuya,Ozawa, Shin-Ichiro,Hirono, Shuichi,Shirahase, Hiroaki

, p. 333 - 351 (2021/04/30)

A novel series of 7-substituted-2-[3-(2-furyl)acryloyl]-6-tetrazolyl-1,2,3,4-tetrahydroisoquinoline derivatives were synthesized to clarify structure–activity relationships for peroxisome proliferator-activated receptor γ (PPARγ) partial agonist activity

Amino-Containing Compounds Which Inhibit Memapsin 2 Beta-Secretase Activity and Methods of Use Thereof

-

Page/Page column 20, (2008/12/05)

The present invention provides novel beta-secretase inhibitors and methods for their use, including methods of treating of Alzheimer's disease.

Design, synthesis and X-ray structure of protein-ligand complexes: Important insight into selectivity of memapsin 2 (β-secretase) inhibitors

Ghosti, Arun K.,Kumaragurubaran, Nagaswamy,Hong, Lin,Lei, Hui,Hussain, Khaja Azhar,Liu, Chun-Feng,Devasamudram, Thippeswamy,Weerasena, Vajira,Turner, Robert,Koelsch, Gerald,Bilcer, Geoffrey,Tang, Jordan

, p. 5310 - 5311 (2007/10/03)

Structure-based design, synthesis, and X-ray structure of protein-ligand complexes of memapsin 2 are described. The inhibitors are designed specifically to interact with S2- and S3-active site residues to provide selectivity over mem

BICYCLIC COMPOUNDS WHICH INHIBIT BETA-SECRETASE ACTIVITY AND METHODS OF USE THEREOF

-

Page/Page column 62, (2010/10/20)

The present invention provides bicyclic beta-secretase inhibitors and methods for their use, including methods of treating of Alzheimer’s disease.

Selective lithiation of 2-methyloxazoles. Applications to pivotal bond constructions in the phorboxazole nucleus

Evans, David A.,Cee, Victor J.,Smith, Thomas E.,Santiago, Keith J.

, p. 87 - 90 (2008/02/11)

(equation presented) R = Alkyl, Vinyl, Aryl 6:7 >95:5 The lithiation of 2-methyloxazoles with alkyllithium and hindered lithium amide bases generally results in the competitive formation of a mixture of 5-lithio-and 2-(lithiomethyl)oxazole isomers. Herein a synthetically useful lithiation method which allows for the selective formation of 2-(lithiomethyl)oxazole is described. Diethylamine has been found to be a kinetically competent proton source that will mediate the equilibration of the kinetically formed 5-lithiooxazole to its more stable 2-(lithiomethyl)oxazole counterpart. Application of this metalation strategy with lithium diethylamide to two important bond constructions relevant to a projected phorboxazole synthesis is presented.

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