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(3-Methoxy-4-propoxyphenyl)methanol is a colorless to yellow liquid chemical compound belonging to the class of phenols. It has a molecular formula of C11H16O3 and a molecular weight of 196.24 g/mol.

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  • 103859-81-0 Structure
  • Basic information

    1. Product Name: (3-METHOXY-4-PROPOXYPHENYL)METHANOL
    2. Synonyms:
    3. CAS NO:103859-81-0
    4. Molecular Formula: C11H16O3
    5. Molecular Weight: 196.25
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103859-81-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 308.2°Cat760mmHg
    3. Flash Point: 140.2°C
    4. Appearance: /
    5. Density: 1.064g/cm3
    6. Vapor Pressure: 0.000299mmHg at 25°C
    7. Refractive Index: 1.512
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (3-METHOXY-4-PROPOXYPHENYL)METHANOL(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3-METHOXY-4-PROPOXYPHENYL)METHANOL(103859-81-0)
    12. EPA Substance Registry System: (3-METHOXY-4-PROPOXYPHENYL)METHANOL(103859-81-0)
  • 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: 103859-81-0(Hazardous Substances Data)

103859-81-0 Usage

Uses

Used in Pharmaceutical Industry:
(3-Methoxy-4-propoxyphenyl)methanol is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. Its potential antioxidant and anti-inflammatory properties make it a promising candidate for medical applications.
Used in Fragrance and Flavoring Industry:
(3-Methoxy-4-propoxyphenyl)methanol is used as a component in the production of fragrances and flavorings, adding unique scents and tastes to various products.

Check Digit Verification of cas no

The CAS Registry Mumber 103859-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,8,5 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 103859-81:
(8*1)+(7*0)+(6*3)+(5*8)+(4*5)+(3*9)+(2*8)+(1*1)=130
130 % 10 = 0
So 103859-81-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O3/c1-3-6-14-10-5-4-9(8-12)7-11(10)13-2/h4-5,7,12H,3,6,8H2,1-2H3

103859-81-0SDS

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 (3-Methoxy-4-propoxyphenyl)methanol

1.2 Other means of identification

Product number -
Other names 3-methoxy-4-propoxy-benzyl 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:103859-81-0 SDS

103859-81-0Relevant articles and documents

Self-Assembly and Host-Guest Interactions of Pd3L2Metallo-cryptophanes with Photoisomerizable Ligands

Britton, Edward,Ansell, Richard J.,Howard, Mark J.,Hardie, Michaele J.

, p. 12912 - 12923 (2021)

New photoswitchable pyridyl-azo-phenyl-decorated tripodal host ligands (Laz) that belong to the cyclotriveratrylene family have been synthesized, and their photoswitching behavior and crystal structures determined. The latter includes a remarkable 7-fold

Guanidine catalyzed aerobic reduction: A selective aerobic hydrogenation of olefins using aqueous hydrazine

Lamani, Manjunath,Guralamata, Ravikumara Siddappa,Prabhu, Kandikere Ramaiah

supporting information; experimental part, p. 6583 - 6585 (2012/07/14)

An efficient aerobic reduction of olefins, internal as well as terminal, is developed using guanidine as an organocatalyst. A remarkable chemoselectivity in reduction has been demonstrated in the presence of a variety of functional groups and protective groups and a selective reduction of a terminal olefin in the presence of an internal olefin is revealed.

Synthesis and biological evaluation of isosteric analogs of mandipropamid for the control of oomycete pathogens

Su, Na,Wang, Zhen-Jun,Wang, Li-Zhong,Zhang, Xiao,Dong, Wei-Li,Wang, Hong-Xue,Li, Zheng-Ming,Zhao, Wei-Guang

, p. 101 - 111 (2012/06/01)

A series of isosteric analogs of mandipropamid were designed and synthesized via 'click chemistry'. The amide bond of mandipropamid was substituted by a 1,2,3-triazole functional group. The bioassay results have indicated that some of the title compounds exhibited moderate fungicidal activity against Pseudoperonospora cubensis, and the activity has been systematically studied as a function of molecular structure. The low activity of the mandipropamid analog that contains a lipid chain is likely due to the presence of a weak hydrogen bond donor in the 1,2,3-triazole. Furthermore, we have performed the molecular modeling and found that N-methylamide could be more effective than amide as the surrogates to 1,2,3-triazole, which ultimately leads to a longer distance (1.1A longer) between the two substitutes in the 1,4-disubstituted 1,2,3-triazole compound.

Substituted γ-phenyl-Δ-lactams and uses related thereto

-

, (2008/06/13)

γ-Phenyl-substituted Δ-lactams are disclosed. They may be formulated into pharmaceutical compositions, and/or used in the treatment or prevention of inflammation or other conditions or disease states.

Substituted gamma-phenyl-delta-lactams and uses related thereto

-

, (2008/06/13)

gamma-Phenyl-substituted Delta-lactams are disclosed. They may be formulated into pharmaceutical compositions, and/or used in the treatment or prevention of inflammation or other conditions or disease states.

Substituted γ-phenyl-Δ-lactones and analogs thereof and uses related thereto

-

, (2008/06/13)

γ-Phenyl-substituted Δ-lactones and analogs thereof, including lactams, are disclosed. They may be formulated into pharmaceutical compositions, and/or used in the treatment or prevention of inflammation or other conditions or disease states.

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