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675149-60-7

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675149-60-7 Usage

Description

(2-Ethyl-5-methyloxazol-4-yl)methanol is an organic compound that belongs to the oxazoles family. It is derived from oxazole, a five-membered aromatic ring containing nitrogen and oxygen atoms. (2-ETHYL-5-METHYLOXAZOL-4-YL)METHANOL consists of a hydroxyl group attached to a 2-ethyl-5-methyloxazol-4-yl moiety, making it an alcohol. It is commonly used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its versatile reactivity and functional group compatibility. Additionally, it may have potential applications in medicinal chemistry and as a chemical intermediate in the production of fine chemicals. Overall, (2-ethyl-5-methyloxazol-4-yl)methanol has diverse uses and plays a crucial role in the development of various chemical products.
Used in Pharmaceutical Industry:
(2-Ethyl-5-methyloxazol-4-yl)methanol is used as a building block for the synthesis of various pharmaceuticals due to its versatile reactivity and functional group compatibility.
Used in Agrochemical Industry:
(2-Ethyl-5-methyloxazol-4-yl)methanol is used as a building block for the synthesis of various agrochemicals due to its versatile reactivity and functional group compatibility.
Used in Organic Compounds Synthesis:
(2-Ethyl-5-methyloxazol-4-yl)methanol is used as a building block for the synthesis of other organic compounds due to its versatile reactivity and functional group compatibility.
Used in Medicinal Chemistry:
(2-Ethyl-5-methyloxazol-4-yl)methanol may have potential applications in medicinal chemistry due to its versatile reactivity and functional group compatibility.
Used in Fine Chemicals Production:
(2-Ethyl-5-methyloxazol-4-yl)methanol is used as a chemical intermediate in the production of fine chemicals due to its versatile reactivity and functional group compatibility.

Check Digit Verification of cas no

The CAS Registry Mumber 675149-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,5,1,4 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 675149-60:
(8*6)+(7*7)+(6*5)+(5*1)+(4*4)+(3*9)+(2*6)+(1*0)=187
187 % 10 = 7
So 675149-60-7 is a valid CAS Registry Number.

675149-60-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-ethyl-5-methyl-1,3-oxazol-4-yl)methanol

1.2 Other means of identification

Product number -
Other names QC-9486

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:675149-60-7 SDS

675149-60-7Downstream Products

675149-60-7Relevant 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

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

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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.

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