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Benzofuran, 2,3,3a,4,5,7a-hexahydro-3,6-dimethyl-, is a chemical compound characterized by its molecular formula C10H14O. It features a benzene ring fused to a furan ring, making it an organic compound with a colorless liquid appearance and a faint odor. Benzofuran, 2,3,3a,4,5,7a-hexahydro-3,6-dimethylis insoluble in water but readily soluble in organic solvents. It serves as a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds, and is utilized in research and development within the chemical and pharmaceutical industries. Due to its potential hazards, careful handling is advised.

70786-44-6

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70786-44-6 Usage

Uses

Used in Pharmaceutical Industry:
Benzofuran, 2,3,3a,4,5,7a-hexahydro-3,6-dimethylis used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, Benzofuran, 2,3,3a,4,5,7a-hexahydro-3,6-dimethylis employed as a precursor in the production of agrochemicals, aiding in the creation of compounds that can enhance crop protection and yield.
Used in Organic Compounds Synthesis:
Benzofuran, 2,3,3a,4,5,7a-hexahydro-3,6-dimethylis utilized as a building block in the synthesis of a range of organic compounds, providing a structural foundation for the development of novel chemical entities with diverse applications.
Used in Research and Development:
Benzofuran, 2,3,3a,4,5,7a-hexahydro-3,6-dimethylis also used in research and development within the chemical and pharmaceutical industries, where it serves as a valuable tool for exploring new chemical reactions and pathways, potentially leading to breakthroughs in material and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 70786-44-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,8 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 70786-44:
(7*7)+(6*0)+(5*7)+(4*8)+(3*6)+(2*4)+(1*4)=146
146 % 10 = 6
So 70786-44-6 is a valid CAS Registry Number.

70786-44-6SDS

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 3,6-dimethyl-2,3,3a,4,5,7a-hexahydro-benzofuran

1.2 Other means of identification

Product number -
Other names 3,7-Dimethyl-4,5,6,7-tetrahydrocumaran

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:70786-44-6 SDS

70786-44-6Relevant academic research and scientific papers

Chemical Tranformation of Terpenoids. V. Acidic Conversions of 10-Hydroxygeraniol and 10-Hydroxynerol Derivatives Leading to Cyclic Monoterpenoids

Kitagawa, Isao,Tsujii, Shinji,Nishikawa, Fumiko,Shibuya, Hirotaka

, p. 2639 - 2651 (2007/10/02)

Acid treatment of 1-O-acetyl-10-hydroxygeraniol (5a), 1-O-methyl-10-hydroxygeraniol (5b), 1-O-acetyl-10-hydroxynerol (6a), and 1-O-methyl-10-hydroxynerol (6b) was investigated under various conditions.It was found that treatment of 5a and 6a with HCOOH gave menth-1-ene-8,9-diol (7), while treatment of 5a, 5b, 6a, or 6b with BF3-etherate in CH2Cl2 furnished two menthofuran-type compounds (9, 10) and two bicyclooct-2-ene derivatives (17, 24).Both 9 and 10 were successfully converted to menthofuran (16) and 17 was converted to a bicyclooctenone derivative (23) which was a key intermediate for a synthesis of juvabione (27).Keywords - geraniol; nerol; 10-hydroxygeraniol; 10-hydroxynerol; 10-hydroxygeraniol derivative; 10-hydroxynerol derivative; uroterpenol; menthofuran; bicyclooct-2-ene derivative

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