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1-Ethenyl-1,2,3,4-tetrahydro-6-methoxy-1-naphthalenol, commonly known as 6-Methoxy-1-tetralol or PMNT, is a naphthalenol derivative that serves as a fragrance ingredient. It is characterized by its clear, colorless to pale yellow liquid form and a floral, sweet odor. PMNT is valued for its pleasant and warm scent, making it a popular choice in the perfumery and cosmetics industry.

3125-36-8

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3125-36-8 Usage

Uses

Used in Fragrance Industry:
1-Ethenyl-1,2,3,4-tetrahydro-6-methoxy-1-naphthalenol is used as a fragrance ingredient for its woody, floral, and slightly fruity note, enhancing the complexity and appeal of perfumes and colognes.
Used in Cosmetic Products:
In the cosmetics industry, 1-Ethenyl-1,2,3,4-tetrahydro-6-methoxy-1-naphthalenol is used as a key component in soaps, detergents, and other products to impart a desirable scent and improve the sensory experience for consumers.
Used in Food Industry:
1-Ethenyl-1,2,3,4-tetrahydro-6-methoxy-1-naphthalenol also serves as a flavoring agent in food products, adding depth and a pleasant aroma to various culinary creations.

Check Digit Verification of cas no

The CAS Registry Mumber 3125-36-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,2 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3125-36:
(6*3)+(5*1)+(4*2)+(3*5)+(2*3)+(1*6)=58
58 % 10 = 8
So 3125-36-8 is a valid CAS Registry Number.

3125-36-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethenyl-6-methoxy-3,4-dihydro-2H-naphthalen-1-ol

1.2 Other means of identification

Product number -
Other names 1,2,3,4-tetrahydro-6-methoxy-1-vinylnaphthalen-1-ol

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:3125-36-8 SDS

3125-36-8Relevant articles and documents

Chemical consequences of fluorine substitution. Part 4. Diels-Alder reactions of fluorinated p-benzoquinones with Dane's diene. Synthesis of fluorinated D-homosteroids

Essers, Michael,Haufe, Guenter

, p. 2719 - 2728 (2007/10/03)

Four fluorinated p-benzoquinones (2) have been reacted with Dane's diene (1) in Diels-Alder reactions and the formed fluorinated D-homosteroids were characterized. The number of products, their stereochemistry and stability depends on the fluorine substitution pattern of the corresponding fluorinated p-benzoquinones. If the p-benzoquinone (2) contains an unfluorinated double bond, this bond reacts faster with diene 1 yielding endo-products selectively. In contrast, [4+2]cycloadditions with 2,6-difluoro (2c) and 2,3,5,6-tetrafluorobenzoquinone (2d) gave the products with exo-orientation of the carbonyl part preferably.

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