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33797-34-1

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33797-34-1 Usage

General Description

(3-Methoxy-2-methylphenyl)methanol is a chemical compound with the molecular formula C9H12O2. It is a colorless liquid with a sweet, floral odor. (3-Methoxy-2-methylphenyl)methanol is often used as a fragrance ingredient in cosmetics, perfumes, and other personal care products. It can also be used as a solvent and as an intermediate in the synthesis of other organic compounds. The compound has low to moderate acute toxicity, with potential irritant effects on the skin and eyes. It is important to handle and use (3-Methoxy-2-methylphenyl)methanol with proper precautions to ensure safety.

Check Digit Verification of cas no

The CAS Registry Mumber 33797-34-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,7,9 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 33797-34:
(7*3)+(6*3)+(5*7)+(4*9)+(3*7)+(2*3)+(1*4)=141
141 % 10 = 1
So 33797-34-1 is a valid CAS Registry Number.

33797-34-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-Methoxy-2-methylphenyl)methanol

1.2 Other means of identification

Product number -
Other names 3-Methoxy-2-methyl-benzylalkohol

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:33797-34-1 SDS

33797-34-1Relevant articles and documents

Vanadium-Catalyzed Oxidative Intramolecular Coupling of Tethered Phenols: Formation of Phenol-Dienone Products

Gilmartin, Philip H.,Kozlowski, Marisa C.

supporting information, p. 2914 - 2919 (2020/04/10)

A mild and efficient method for the vanadium-catalyzed intramolecular coupling of tethered free phenols is described. The corresponding phenol-dienone products are prepared directly in good yields with low catalyst loadings. Electronically diverse tethered phenol precursors are well tolerated, and the catalytic method was effectively applied as the key step in syntheses of three natural products and a synthetically useful morphinan alkaloid precursor.

α-Ketocarbenium Ions Derived from Orthoquinone-Containing Polycyclic Aromatic Compounds

Urakawa, Kazuki,Kawabata, Yuta,Matsuda, Masaki,Sumimoto, Michinori,Ishikawa, Hayato

supporting information, p. 2534 - 2537 (2018/05/22)

α-Ketocarbenium ions derived from synthesized orthoquinone-containing polycyclic aromatic compounds were generated in the presence of Br?nsted acids such as sulfuric acid, trifluoromethanesulfonic acid, and fluorosulfonic acid. The prepared α-ketocarbeniu

HETEROCYCLIC CARBOXYLIC ACIDS AS ACTIVATORS OF SOLUBLE GUANYLATE CYCLASE

-

Paragraph 0312-0313, (2016/02/18)

The present invention relates to compounds of formula I: and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R5, R6, R7, R8, R9, B, V, W, X, Y, Z and m are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.

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