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(2-Methylbenzo[d]oxazol-5-yl)Methanol is a chemical compound characterized by its molecular formula C9H9NO2. It is a derivative of benzo[d]oxazole, a heterocyclic aromatic organic compound, with an additional methanol group attached to its structure, classifying it as an alcohol. (2-Methylbenzo[d]oxazol-5-yl)Methanol may serve as a building block for the synthesis of more complex organic molecules, potentially finding applications in various fields such as pharmaceuticals, agrochemicals, and materials science.

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  • 136663-38-2 Structure
  • Basic information

    1. Product Name: (2-Methylbenzo[d]oxazol-5-yl)Methanol
    2. Synonyms: (2-Methylbenzo[d]oxazol-5-yl)Methanol
    3. CAS NO:136663-38-2
    4. Molecular Formula: C9H9NO2
    5. Molecular Weight: 163.17326
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 136663-38-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: (2-Methylbenzo[d]oxazol-5-yl)Methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-Methylbenzo[d]oxazol-5-yl)Methanol(136663-38-2)
    11. EPA Substance Registry System: (2-Methylbenzo[d]oxazol-5-yl)Methanol(136663-38-2)
  • 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: 136663-38-2(Hazardous Substances Data)

136663-38-2 Usage

Uses

Used in Pharmaceutical Industry:
(2-Methylbenzo[d]oxazol-5-yl)Methanol is used as a chemical intermediate for the synthesis of pharmaceutical compounds. Its unique structure allows it to be a potential candidate for the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Agrochemical Industry:
In the agrochemical sector, (2-Methylbenzo[d]oxazol-5-yl)Methanol may be utilized as a precursor for the creation of novel agrochemicals, such as pesticides or herbicides. Its ability to form complex molecules could contribute to the development of more effective and targeted agricultural products.
Used in Materials Science:
(2-Methylbenzo[d]oxazol-5-yl)Methanol can be employed as a component in the development of advanced materials with specific properties. Its incorporation into polymers or other materials could lead to the creation of materials with improved characteristics, such as enhanced stability, reactivity, or selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 136663-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,6,6 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 136663-38:
(8*1)+(7*3)+(6*6)+(5*6)+(4*6)+(3*3)+(2*3)+(1*8)=142
142 % 10 = 2
So 136663-38-2 is a valid CAS Registry Number.

136663-38-2Downstream Products

136663-38-2Relevant articles and documents

1H-PYRAZOLO[4,3-B]PYRIDINES AS PDE1 INHIBITORS

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Paragraph 0717-0718, (2019/07/10)

The present invention provides 1H-pyrazolo[4,3-b]pyridines of formula (I) as PDE1 inhibitors and their use as a medicament, in particular for the treatment of neurodegenerative disorders and psychiatric disorders.

PYRAZOLOPYRIDINE PYRAZOLOPYRIMIDINE AND RELATED COMPOUNDS

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Paragraph 1223; 1224, (2015/11/25)

In one aspect this invention relates generally to compounds of Formula: and sub-formulas thereof, or a tautomer of each thereof, a pharmaceutically acceptable salt of each thereof, or a pharmaceutically acceptable solvate of each of the foregoing, where X1, L1, L3, and R3 are described herein.

Palladium-catalyzed direct hydroxymethylation of aryl halides and triflates with potassium acetoxymethyltrifluoroborate

Murai, Norio,Yonaga, Masahiro,Tanaka, Keigo

supporting information; experimental part, p. 1278 - 1281 (2012/04/23)

Suzuki-Miyaura cross-coupling reactions of aryl halides and triflates with potassium acetoxymethyltrifluoroborate afforded the corresponding aryl and heteroaryl methanol products in moderate to excellent yields.

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