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(2-Methoxy-6-Methylphenyl)Methanol, also known as veratryl alcohol, is a chemical compound characterized by its molecular formula C9H12O2. It presents as a colorless, crystalline solid with a distinctive sweet, floral scent. This versatile compound is recognized for its potential antioxidant and antimicrobial properties, which contribute to its value across a spectrum of industries.

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  • 89244-39-3 Structure
  • Basic information

    1. Product Name: (2-Methoxy-6-Methylphenyl)Methanol
    2. Synonyms: (2-Methoxy-6-Methylphenyl)Methanol
    3. CAS NO:89244-39-3
    4. Molecular Formula: C9H12O2
    5. Molecular Weight: 152.19038
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 89244-39-3.mol
  • Chemical Properties

    1. Melting Point: 51-52 °C
    2. Boiling Point: 259.0±25.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.060±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 14.44±0.10(Predicted)
    10. CAS DataBase Reference: (2-Methoxy-6-Methylphenyl)Methanol(CAS DataBase Reference)
    11. NIST Chemistry Reference: (2-Methoxy-6-Methylphenyl)Methanol(89244-39-3)
    12. EPA Substance Registry System: (2-Methoxy-6-Methylphenyl)Methanol(89244-39-3)
  • 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: 89244-39-3(Hazardous Substances Data)

89244-39-3 Usage

Uses

Used in Organic Synthesis:
(2-Methoxy-6-Methylphenyl)Methanol is utilized as a fundamental building block in the realm of organic synthesis. Its unique structure allows for the creation of a variety of complex organic compounds, making it indispensable in this field.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, (2-Methoxy-6-Methylphenyl)Methanol serves as a crucial precursor. Its role in the synthesis of various medicinal compounds underscores its importance in developing new drugs and treatments.
Used in Fragrance Production:
The naturally sweet, floral odor of (2-Methoxy-6-Methylphenyl)Methanol makes it a favored ingredient in the fragrance industry. It is used to create and enhance the scent profiles of numerous perfumes and scented products.
Used in Chemical Reactions:
(2-Methoxy-6-Methylphenyl)Methanol is also a common reagent in chemical reactions, particularly within the domain of organic chemistry. Its reactivity and stability make it a reliable choice for various laboratory procedures and industrial processes.
Used in Cosmetics and Personal Care Products:
The antioxidant and antimicrobial properties of (2-Methoxy-6-Methylphenyl)Methanol render it a valuable addition to the cosmetics and personal care sector. It is often incorporated into products to enhance their shelf life and provide additional benefits to users, such as skin protection and nourishment.

Check Digit Verification of cas no

The CAS Registry Mumber 89244-39-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,4 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89244-39:
(7*8)+(6*9)+(5*2)+(4*4)+(3*4)+(2*3)+(1*9)=163
163 % 10 = 3
So 89244-39-3 is a valid CAS Registry Number.

89244-39-3SDS

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 (2-Methoxy-6-methylphenyl)methanol

1.2 Other means of identification

Product number -
Other names 2-Methoxy-6-methylbenzyl alcohol

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:89244-39-3 SDS

89244-39-3Relevant articles and documents

FXR receptor agonist

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, (2019/02/10)

The present invention discloses an FXR receptor agonist, belongs to the technical field of medicine, and particularly relates to a compound represented by a formula (I), a pharmaceutically acceptablesalt, an ester or a stereoisomer thereof, wherein R, R, R, M, L, L1, W, A , B, Q, m and n are defined in the specification. The present invention further relates to a preparation method of the compound, a pharmaceutical preparation, and applications in preparation of drugs for treatment and/or prevention of nonalcoholic fatty liver disease, primary biliary cirrhosis, lipid metabolism disorder, diabetic complication, malignant tumors and other related diseases mediated by FXR receptors. The formula I is defined in the specification.

Imidazo[1,2-a]pyridine derivatives, methods of preparing the same and use thereof

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, (2017/10/31)

The present invention relates to an imidazo[1,2-a]pyridine derivative, and more specifically, to an imidazo[1,2-a]pyridine derivative having excellent gastric acid secretion inhibitory activity, a method of preparing the same, and a use thereof. The imidazo[1,2-a]pyridine derivative according to the present invention has gastric acid secretion inhibitory activity, and can be usefully applied for preventing or treating gastrointestinal inflammatory diseases or gastric-related diseases.(AA) Control group(BB) Example 6(CC) Example 7(DD) Embodiment 11COPYRIGHT KIPO 2017

2-BENZYL-BENZIMIDAZOLE COMPLEMENT FACTOR B INHIBITORS AND USES THEREOF

-

Page/Page column 48, (2015/05/19)

The present invention provides a compound of formula (I) a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical comp

N-PYRAZOLYL CARBOXAMIDES AS CRAC CHANNEL INHIBITORS

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Page/Page column 75-76, (2010/11/05)

The present invention relates to amide compounds, processes for their preparation, pharmaceutical compositions containing these compounds and to their use in the treatment of disorders, conditions or disorders such as allergic disorders, inflammatory disorders and disorders of the immune system.

Regioselective reductive opening of substituted phthalans: synthetic applications

García, Daniel,Foubelo, Francisco,Yus, Miguel

, p. 4275 - 4286 (2008/09/20)

The reductive opening of substituted phthalans 6, 11, 12, 20, 21 and 28 with lithium and a catalytic amount of DTBB leads to the formation of corresponding functionalised organolithium intermediates 8, 15, 16, 23, 25 and 29+30 in a regioselective manner. The further reaction of these dianions with different electrophiles, mainly carbonyl compounds, gives the expected functionalised benzylic alcohols 9, 17, 18, 24, 26 and 31+32. The observed stereochemistry can be easily explained taking into account the values of the electron densities deduced by semiempirical PM3 calculations.

Phytochemical study on American plants I. Two new phenol glucosides, together with known biflavones and diterpene, from leaves of Juniperus occidentalis Hook.

Nakanishi, Tsutomu,Inatomi, Yuka,Murata, Hiroko,Iida, Naoki,Inada, Akira,Lang, Frank A,Murata, Jin

, p. 1358 - 1361 (2007/10/03)

Two new phenol glucosides termed juniperosides I (1) and II (2) were isolated, together with known two biflavones, cupressuflavone and amentoflavone and a diterpene, 3beta-hydroxy sandaracopimaric acid, from leaves of Juniperus occidentalis HOOK. (Cupress

A facile synthesis of [14C]enadoline [(5R)-(5α,7α,8β)]-N-methyl-N-[7-(1-pyrrolidinyl)-1-oxospiro[4,5] dec-8-yl]-4-benzofuranacetamide

Pu,Scripko,Huang

, p. 1183 - 1191 (2007/10/03)

4-Chloromethylbenzofuran (10) was synthesized from 2,3-dimethylanisole in 7 steps. The corresponding Grignard reagent prepared from magnesium anthracene complex reacts with 14CO2, SOCl2, and PD130812 successively to give [

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