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CAS

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166180-75-2

Isoxazole, 3-ethoxy-4-methyl-5-(2-thiazolyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 166180-75-2 Structure

  • Basic information

    1. Product Name: Isoxazole, 3-ethoxy-4-methyl-5-(2-thiazolyl)- (9CI)
    2. Synonyms: Isoxazole, 3-ethoxy-4-methyl-5-(2-thiazolyl)- (9CI)
    3. CAS NO:166180-75-2
    4. Molecular Formula: C9H10N2O2S
    5. Molecular Weight: 210.2529
    6. EINECS: N/A
    7. Product Categories: ETHOXY
    8. Mol File: 166180-75-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 373.6±52.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.235±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 0.39±0.10(Predicted)
    10. CAS DataBase Reference: Isoxazole, 3-ethoxy-4-methyl-5-(2-thiazolyl)- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Isoxazole, 3-ethoxy-4-methyl-5-(2-thiazolyl)- (9CI)(166180-75-2)
    12. EPA Substance Registry System: Isoxazole, 3-ethoxy-4-methyl-5-(2-thiazolyl)- (9CI)(166180-75-2)

  • 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: 166180-75-2(Hazardous Substances Data)

166180-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 166180-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,1,8 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 166180-75:
(8*1)+(7*6)+(6*6)+(5*1)+(4*8)+(3*0)+(2*7)+(1*5)=142
142 % 10 = 2
So 166180-75-2 is a valid CAS Registry Number.

166180-75-2SDS

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 3-ethoxy-4-methyl-5-(2-thiazolyl)isoxazol

1.2 Other means of identification

Product number -
Other names 3-Ethoxy-4-methyl-5-thiazol-2-yl-isoxazole

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:166180-75-2 SDS

166180-75-2Downstream Products

166180-75-2Relevant articles and documents

5-Arylisoxazol-4-yl-substituted 2-amino carboxylic acid compounds

-

, (2008/06/13)

2-Aminocarboxylic acid compounds substituted with 5-arylisoxazol-4-yl or 5-arylisothiazol-4-yl and having general formula (I), wherein A is a bond or a spacer group; B is a group -CH(NR'R'')-COOH wherein R' and R'' are independently hydrogen or C1-6 alkyl, or B is a group of formula (II), wherein R2, R3 and R4 are substituents; or R3 and R4 or R4 and R2 are connected in order to form a ring; E is O, S, COO, (CH2)n-COO, O-(CH2)n-COO or S-(CH2)n-COO wherein n is 1-6, 5-tetrazolyl, 5-tetrazolyl-C1-6 alkyl, 3-hydroxyisoxazolyl or 3-hydroxyisoxazolyl-C1-6 alkyl; D is O or S; and R1 is an optionally substituted aryl or heteroaryl group; are excitatory amino acid receptor ligands useful in the treatment of cerebral ischaemia, Huntington's disease, epileptic disorders, Parkinson's disease, Alzheimer's disease, schizophrenia, pain, depression and anxiety.

Heteroaryl analogues of AMPA. Synthesis and quantitative structure- activity relationships

Bang-Andersen, Benny,Lenz, Sibylle M.,Skj?rb?k, Niels,S?by, Karina K.,Hansen, Hans O.,Ebert, Bjarke,B?ges?, Klaus P.,Krogsgaard-Larsen, Povl

, p. 2831 - 2842 (2007/10/03)

A number of 3-isoxazolol bioisosteres, 7a-i, of (S)-glutamic acid (Glu), in which the methyl group of (RS)-2-amino-3-(3-hydroxy-5-methylisoxazol-4- yl)propionic acid (AMPA, 1) was replaced by different 5-membered heterocyclic rings, were synthesized. Comp

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