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3-Benzofurancarboxaldehyde, 2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 55581-61-8 Structure
  • Basic information

    1. Product Name: 3-Benzofurancarboxaldehyde, 2-methyl-
    2. Synonyms: 3-Benzofurancarboxaldehyde, 2-methyl-
    3. CAS NO:55581-61-8
    4. Molecular Formula: C10H8O2
    5. Molecular Weight: 160.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 55581-61-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-Benzofurancarboxaldehyde, 2-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Benzofurancarboxaldehyde, 2-methyl-(55581-61-8)
    11. EPA Substance Registry System: 3-Benzofurancarboxaldehyde, 2-methyl-(55581-61-8)
  • 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: 55581-61-8(Hazardous Substances Data)

55581-61-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55581-61-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,5,8 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55581-61:
(7*5)+(6*5)+(5*5)+(4*8)+(3*1)+(2*6)+(1*1)=138
138 % 10 = 8
So 55581-61-8 is a valid CAS Registry Number.

55581-61-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1-benzofuran-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-Methylbenzofuran-3-carbaldehyde

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:55581-61-8 SDS

55581-61-8Relevant articles and documents

Synthesis of Chiral Polycyclic Tetrahydrocarbazoles by Enantioselective Aminocatalytic Double Activation of 2-Hydroxycinnamaldehydes with Dienals

Ming, Yong-Chao,Lv, Xue-Jiao,Liu, Ming,Liu, Yan-Kai

, p. 6515 - 6519 (2021/09/02)

An efficient aminocatalytic enantioselective double-activation strategy has been developed that combines several different aminocatalytic modes in a cascade process, such as iminium ion, vinylogous iminium ion, trienamine, and dienamine activations. By using this strategy, 2-hydroxycinnamaldehydes worked well with various dienals via [4 + 2] cycloaddition and the oxa-Michael reaction-initiated cascade, respectively, leading to chiral polycyclic tetrahydrocarbazole and chromane derivatives with excellent diastereo- and enantioselectivities.

NOVEL COMPOUNDS AND THEIR USE

-

Page/Page column 69-70, (2021/06/26)

The present invention provides compounds of the general formula (I) or a pharmaceutically acceptable prodrugs, salts and/or solvates thereof, wherein LHS is selected from the group consisting of LHSa and LHSb And wherein, the asterisk (*) marks the point of attachment; These compounds exhibit antibacterial activity against Gram-negative and Gram-positive bacteria, especially S. aureus, E. coli, K. pneumoniae and A. baumannii. Pharmaceutical compositions containing these compounds, therapeutic uses thereof and methods for manufacturing the same are also provided.

Palladium-catalysed annulative allylic alkylation for the synthesis of benzannulated heteroarenes

Yadav, Sonu,Ramasastry

supporting information, p. 77 - 80 (2021/01/13)

A conceptually novel intramolecular allylic alkylation strategy is developed for the synthesis of carbazoles and dibenzothiophenes. In an unusual event, palladium catalyses the formation of π-allylpalladium complexes of the respective (2-methylindol-3-yl)allyl acetates and subsequently facilitates the benzannulation process. This journal is

ANTIBIOTIC COMPOUNDS, METHODS OF MANUFACTURING THE SAME, PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME AND USES THEREOF

-

Paragraph 00312; 00313, (2020/06/05)

The present invention provides compounds of the general structure (I), which are suitable as antibiotic compounds for the treatment of N. gonorrhoeae infections and related infections.

Cyclopenta[b]annulation of Heteroarenes by Organocatalytic γ′[C(sp3)?H] Functionalization of Ynones

Raghu, Moluguri,Grover, Jagdeep,Ramasastry

, p. 18316 - 18321 (2016/12/16)

A new approach for the cyclopenta[b]annulation of heteroarenes through metal-free and directing-group-free γ′[C(sp3)?H] functionalization and intramolecular hydroalkylation of ynones has been developed. In an unprecedented event, nucleophilic addition of an organophosphine to the designed ynones triggers γ′[C(sp3)?H] functionalization, leading to the formation of heteroaryl-based ortho-quinodimethane (oQDM) intermediates that undergo carbocyclization to provide cyclopentannulated heteroarenes in good yields and excellent stereoselectivities. Deuterium-labeling experiments substantiated the proposed reaction mechanism as well as the speculated epimerization.

Vinylindenes and Some Heteroanalogues in the Diels-Alder Reaction. X Dibenzofurans from 3-Vinylbenzofurans

Pearson, James R.,Porter, Quentin N.

, p. 1085 - 1095 (2007/10/02)

3-Vinylbenzofuran, 3-isopropenylbenzofuran and 2-methyl-3-vinylbenzofuran give normal adducts with ethenetetracarbonitrile, accompanied, in the case of the last named diene, by the isomeric cyclobutane.Normal adducts also result from these dienes and 4-phenyl-1,2,4-triazoline-3,5-dione, and from 3-vinylbenzofuran and both maleic anhydride and N-phenylmaleimide. 3-Vinylbenzofuran gives the rearranged adduct dimethyl 1,2-dihydrodibenzofuran-3,4-dicarboxylate with dimethyl acetylenedicarboxylate.

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