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3-methyl-2-nitro-4,4a,5,6-tetrahydronaphtho[2,3-b]furan is a complex organic chemical compound with the molecular formula C12H13NO3. It features a naphthalene core with a furan ring fused to it, and it has a methyl group at the 3-position and a nitro group at the 2-position. 3-methyl-2-nitro-4,4a,5,6-tetrahydronaphtho[2,3-b]furan is characterized by its unique structure, which includes a partially saturated ring system (tetrahydro) and a bridged ring structure (naphtho[furan]). Due to its specific functional groups and structural features, it may have potential applications in various chemical and pharmaceutical industries. However, further research and analysis are required to determine its specific uses and properties.

86295-62-7

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86295-62-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86295-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,9 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86295-62:
(7*8)+(6*6)+(5*2)+(4*9)+(3*5)+(2*6)+(1*2)=167
167 % 10 = 7
So 86295-62-7 is a valid CAS Registry Number.

86295-62-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name nitro-2 methyl-3 tetrahydro-5,6,7,8 naphto<2,3-b>furanne

1.2 Other means of identification

Product number -
Other names 3-methyl-2-nitro-5,6,7,8-tetrahydronaphtho&lt

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:86295-62-7 SDS

86295-62-7Relevant academic research and scientific papers

Research on nitro-derivatives of biological interest. XXVIII. Synthesis of hydrogenated analogs of 2-nitronaphthofuranes and activities against microorganisms

Einhorn,Demerseman,Rene,et al.

, p. 79 - 84 (2007/10/02)

The authors describe the various ways of transforming 5.6.7.8-tetrahydro 1- and 2-naphthols to 2-nitro 6.7.8.9-tetrahydronaphtho[2.1-b]furan, 2-nitro 5.6.7.8-tetrahydronaphtho[2.3-b]furan and 2-nitro 6.7.8.9-tetrahydronaphtho[1.2-b]furan as well as their derivatives methylated on the furan ring. Although the hydrogenated analogues of 2-nitronaphthofurans are less active than 2-nitronaphthofurans against bacteria, they tend to be more efficacious against protozoa. Their methylated derivatives are particularly efficient against these latter.

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