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4(5H)-Benzofuranone, 6,7-dihydro-3-methyl- is an organic compound with the chemical formula C9H10O2. It is a derivative of benzofuran, a heterocyclic aromatic organic compound consisting of a benzene ring fused to a furan ring. The compound is characterized by the presence of a 6,7-dihydro structure, which means that the furan ring is partially saturated, and a methyl group attached to the 3-position of the benzofuranone structure. 4(5H)-Benzofuranone, 6,7-dihydro-3-methyl- is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure and properties.

6906-61-2

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6906-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6906-61-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,0 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6906-61:
(6*6)+(5*9)+(4*0)+(3*6)+(2*6)+(1*1)=112
112 % 10 = 2
So 6906-61-2 is a valid CAS Registry Number.

6906-61-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-6,7-dihydro-5H-1-benzofuran-4-one

1.2 Other means of identification

Product number -
Other names 3-methyl-6,7-dihydro-5H-benzofuran-4-one

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 -
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More Details:6906-61-2 SDS

6906-61-2Relevant academic research and scientific papers

Total synthesis of marine furanosesquiterpenoids, tubipofurans

Ojida,Tanoue,Kanematsu

, p. 5970 - 5976 (2007/10/02)

The first total syntheses of marine furanosesquiterpenoids, tubipofuran (1) and 15-acetoxytubipofuran (2), have been achieved via the common intermediate 3. The syntheses were begun by our newly improved fused 3-methylfuran construction method by the reac

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