19672-02-7

• 

• Basic information

  1. Product Name: 2-ETHYL-5-METHOXYPHENOL
  2. Synonyms: 2-ETHYL-5-METHOXYPHENOL;2-ETHYL-6-METHOXYPHENOL;2-Aethyl-5-methoxy-phenol
  3. CAS NO:19672-02-7
  4. Molecular Formula: C₉H₁₂O₂
  5. Molecular Weight: 152.19
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 19672-02-7.mol
  9. Article Data: 7

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 256.956 °C at 760 mmHg
  3. Flash Point: 121.614 °C
  4. Appearance: /
  5. Density: 1.052 g/cm³
  6. Refractive Index: N/A
  7. Storage Temp.: 2-8°C
  8. Solubility: N/A
  9. CAS DataBase Reference: 2-ETHYL-5-METHOXYPHENOL(CAS DataBase Reference)
  10. NIST Chemistry Reference: 2-ETHYL-5-METHOXYPHENOL(19672-02-7)
  11. EPA Substance Registry System: 2-ETHYL-5-METHOXYPHENOL(19672-02-7)

• 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: 19672-02-7(Hazardous Substances Data)

• Suppliers
• Usage
• SDS
• Upstream product
• Downstream Products
• Article

19672-02-7 Suppliers

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• Phenol,2-ethyl-5-methoxy-

  Cas No: 19672-02-7

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• 10 Gram

• 500 Kilogram/Month

• Zibo Hangyu Biotechnology Development Co., Ltd
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• Phenol,2-ethyl-5-methoxy-

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• Antimex Chemical Limied
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• 2-ETHYL-5-METHOXYPHENOL

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• Hangzhou Fandachem Co.,Ltd
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• 2-Ethyl-5-methoxyphenol

  Cas No: 19672-02-7

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• 10 Milligram

• Amadis Chemical Co., Ltd.
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• 2-ETHYL-5-METHOXYPHENOL

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• Chemical Technology Co.,LTD
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• 2-ETHYL-5-METHOXYPHENOL

  Cas No: 19672-02-7

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• Shanghai Run-Biotech Co., Ltd.
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• Phenol,2-ethyl-5-methoxy-

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• Fontarome Chemical, Inc.
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19672-02-7 Usage

General Description

2-Ethyl-5-methoxyphenol, also known as eugenol methyl ether, is a chemical compound with a molecular formula C11H16O2. It is a pale yellow liquid with a sweet, spicy odor, commonly found in essential oils such as clove oil and basil oil. 2-Ethyl-5-methoxyphenol is widely used in the fragrance and flavor industry as a flavoring agent and fragrance ingredient due to its pleasant aroma and taste. It has also been used in traditional medicine for its analgesic and anti-inflammatory properties. Additionally, it has potential applications in pharmaceuticals, insecticides, and as a food preservative due to its antimicrobial activity.

Check Digit Verification of cas no

The CAS Registry Mumber 19672-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,6,7 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19672-02:
(7*1)+(6*9)+(5*6)+(4*7)+(3*2)+(2*0)+(1*2)=127
127 % 10 = 7
So 19672-02-7 is a valid CAS Registry Number.

19672-02-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-ETHYL-5-METHOXYPHENOL

1.2 Other means of identification

Product number	-
Other names	5-methoxy-2-ethyl-phenol

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:19672-02-7 SDS

19672-02-7Upstream product

• 108-46-3 recorcinol 
• 89-84-9 2',4'-dihydroxy-4-acetophenone 
• 150-19-6 O-methylresorcine 
• 64-17-5 ethanol 
• 552-41-0 1-(2-hydroxy-4-methoxyphenyl)ethanone 

19672-02-7Downstream Products

• 55157-48-7 2-ethyl-5-methoxycyclohexa-2,5-diene-1,4-dione 
• 877130-72-8 4-bromo-5-methoxy-2-ethyl-phenol 
• 1484-73-7 6-Ethyl-7-hydroxy-4-methylcumarin 
• 511277-71-7 2-(4-benzyloxy-5-ethyl-2-methoxy-phenyl)-6-(2,5-dimethyl-pyrrol-1-yl)-pyridine 
• 511277-75-1 4-[6-(2,5-dimethyl-pyrrol-1-yl)-pyridin-2-yl]-6-ethyl-3-methoxyphenol 
• 511277-69-3 4-benzyloxy-5-ethyl-2-methoxy-phenylboronic acid 
• 511277-77-3 4-(6-amino-pyridin-2-yl)-2-ethyl-5-methoxyphenol 
• 511277-67-1 5-benzyloxy-2-bromo-4-ethyl-1-methoxybenzene 
• 511277-65-9 3-benzyloxy-4-ethyl-1-methoxybenzene 

19672-02-7Relevant articles and documents

Primulin derivative as well as synthesis method and application of primulin derivative

-

Paragraph 0021, (2018/01/11)

The invention discloses a primulin derivative with antibacterial activity shown as the structural general formula (I), wherein R is selected from C2-C20 alkyls. The primulin derivative is prepared from raw materials including m-dihydroxybenzene and a fatty acid derivative by the steps: carrying out Friedel-Crafts acylation and methylation to synthesize a paeonol derivative, and carrying out oxidization after carrying out carbonyl reduction. The primulin derivative has good antibacterial activity and can be used as a potential antibacterial agent.

Dehydrative C-H alkylation and alkenylation of phenols with alcohols: Expedient synthesis for substituted phenols and benzofurans

Lee, Dong-Hwan,Kwon, Ki-Hyeok,Yi, Chae S.

supporting information; experimental part, p. 7325 - 7328 (2012/06/16)

A well-defined cationic Ru-H complex catalyzes the dehydrative C-H alkylation reaction of phenols with alcohols to form ortho-substituted phenol products. Benzofuran derivatives are efficiently synthesized from the dehydrative C-H alkenylation and annulation reaction of phenols with 1,2-diols. The catalytic C-H coupling method employs cheaply available phenols and alcohols, exhibits a broad substrate scope, tolerates carbonyl and amine functional groups, and liberates water as the only byproduct.

Substituted 6-phenyl-pyridin-2-ylamines: Selective and potent inhibitors of neuronal nitric oxide synthase

Nason, Deane M.,Heck, Steven D.,Bodenstein, Mathew S.,Lowe III, John A.,Nelson, Robert B.,Liston, Dane R.,Nolan, Charles E.,Lanyon, Lorraine F.,Ward, Karen M.,Volkmann, Robert A.

, p. 4511 - 4514 (2007/10/03)

The synthesis and nNOS and eNOS activity of 6-(4-(dimethylaminoalkyl)-/6- (4-(dimethylaminoalkoxy)-5-ethyl-2-methoxyphenyl)-pyridin-2-ylamines and 6-(4-(dimethylaminoalkyl)-/6-(4-(dimethylaminoalkoxy)-2,5-dimethoxyphenyl) -pyridin-2-ylamines 1-8 are described. These compounds are potent inhibitors of the human nNOS isoform.

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