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Phenol, 2-cyclopropyl-6-methyl(9CI) is a chemical compound that is a derivative of phenol with a cyclopropyl and methyl group attached to the aromatic ring. It is commonly used in the production of various industrial chemicals, pharmaceuticals, and pesticides. Phenol, 2-cyclopropyl-6-methyl(9CI) has demonstrated biological activity, including antimicrobial and antifungal properties. However, it is important to handle this chemical with care as it can be irritating to the skin, eyes, and respiratory tract, and can be toxic if ingested or inhaled in large amounts. Proper safety precautions should be taken when working with Phenol, 2-cyclopropyl-6-methyl- (9CI) to minimize the risk of exposure and harm.

499236-68-9

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499236-68-9 Usage

Uses

Used in Pharmaceutical Industry:
Phenol, 2-cyclopropyl-6-methyl(9CI) is used as an intermediate in the synthesis of various pharmaceuticals due to its unique chemical structure and biological activity. Its antimicrobial and antifungal properties make it a valuable component in the development of new drugs and treatments.
Used in Pesticide Industry:
Phenol, 2-cyclopropyl-6-methyl(9CI) is also used in the production of pesticides, where its antimicrobial and antifungal properties can help control and prevent the growth of harmful organisms that can damage crops and other plants.
Used in Industrial Chemical Production:
Phenol, 2-cyclopropyl-6-methyl(9CI) serves as a key intermediate in the synthesis of various industrial chemicals, contributing to the development of new materials and products across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 499236-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,9,2,3 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 499236-68:
(8*4)+(7*9)+(6*9)+(5*2)+(4*3)+(3*6)+(2*6)+(1*8)=209
209 % 10 = 9
So 499236-68-9 is a valid CAS Registry Number.

499236-68-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Cyclopropyl-6-methylphenol

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:499236-68-9 SDS

499236-68-9Downstream Products

499236-68-9Relevant academic research and scientific papers

Pyridine N-oxidation derivative as well as preparation method and application thereof

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Paragraph 1273-1279, (2019/08/06)

The invention relates to a pyridine N-oxidation derivative as well as a preparation method and an application thereof, in particular to a compound shown in a general formula (I), a preparation methodof the compound, pharmaceutical composition containing the compound and an application of the compound as a BRD4 inhibitor in treating related diseases such as cancer, inflammation, chronic liver diseases, diabetes, cardiovascular diseases, AIDS and the like, wherein in the general formula (I), all substituent groups are the same as definitions in the description.

2 - - 2, 3 - Dihydrobenzofuran compounds 3 - halomethyl [...] compound and method of manufacturing (by machine translation)

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, (2018/04/11)

[Problem] under mild conditions (temperature, such as reagents and solvents), reaction can be effectively suppressed, and the reagent and the solvent to be used can be also suppressed, the safety can be enhanced and increased productivity in industrial production, production of compound 2 - [...], and excellent in the manufacturing and 3 - halomethyl - 2, 3 - dihydrobenzofuran compound. (2) A compound represented by the following formula [a], metal M1 , Metal M1 Metal salt, or an organic metal compound M2 The reaction, (1) a compound represented by formula a, - 2, 3 - dihydrobenzofuran (2) is represented by formula 2 - production of compound 3 - halomethyl [...] and compound. [1 A] In the formulas, R1 - R4 Each independently represents a substituent, X is a chlorine atom, a bromine atom or an iodine atom. [Drawing] no (by machine translation)

5H-PYRROLO[3,4-£>]PYRAZIN-7-AMINE DERIVATIVES INHIBITORS OF BETA-SECRETASE

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, (2011/02/24)

The present invention relates to novel compounds of formula (I) and their pharmaceutical compositions. In addition, the present invention relates to therapeutic methods for the treatment and/or prevention of Aβ-related pathologies such as Downs syndrome, β- amyloid angiopathy such as but not limited to cerebral amyloid angiopathy or hereditary cerebral hemorrhage, disorders associated with cognitive impairment such as but not limited to MCI ("mild cognitive impairment"), Alzheimer Disease, memory loss, attention deficit symptoms associated with Alzheimer disease, neurodegeneration associated with diseases such as Alzheimer disease or dementia including dementia of mixed vascular and degenerative origin, pre-senile dementia, senile dementia and dementia associated with Parkinson's disease, progressive supranuclear palsy or cortical basal degeneration.

NEW COMPOUNDS 574

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Page/Page column 25, (2010/06/13)

The present invention relates to novel compounds of formula (I) and their pharmaceutical compositions. In addition, the present invention relates to therapeutic methods for the treatment and/or prevention of Aβ-related pathologies such as Downs syndrome,

PROCESS FOR PRODUCING CYCLOPROPYLPHENOL DERIVATIVE

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Page/Page column 84, (2008/06/13)

A method of easily synthesizing a cyclopropylphenol derivative. The method, which is a process for producing a cyclopropylphenol derivative represented by the general formula (10): [wherein R1, R2, R3, and R4 each independently is hydrogen, etc.; Z is hydrogen, etc.; and Y1, Y2, and Y3 each independently is hydrogen, etc.], comprises reacting a compound represented by the general formula (7): [wherein the symbols have the same meanings as defined above; X is halogeno; and V is hydrogen, etc.] with a metal, metal salt, or organometallic compound represented by the general formula M2 (8) to obtain a compound represented by the general formula (9): [wherein the symbols have the same meanings as defined above]. When V is a -W-R5 group, hydrolysis is further conducted. Thus, a compound of the general formula (10) is obtained.

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