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2,4-DibroModibenzo[b,d]furan-3-aMine is a chemical compound that belongs to the dibenzofuran class, characterized by its unique structure as a brominated derivative with a primary amine functional group. 2,4-DibroModibenzo[b,d]furan-3-aMine exhibits distinctive properties due to the presence of bromine, making it a promising candidate for research and development in various scientific fields, particularly in organic synthesis and medicinal chemistry.

133953-35-2

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133953-35-2 Usage

Uses

Used in Organic Synthesis:
2,4-DibroModibenzo[b,d]furan-3-aMine is used as a building block in organic synthesis for the creation of more complex compounds. Its unique structure and the presence of bromine atoms make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,4-DibroModibenzo[b,d]furan-3-aMine is utilized as a potential lead compound for the development of new drugs. Its chemical properties and structural features can be exploited to design and optimize therapeutic agents targeting various diseases and conditions.
Used in Chemical Reactions:
The presence of bromine in 2,4-DibroModibenzo[b,d]furan-3-aMine endows it with unique reactivity, making it a useful reactant in certain chemical reactions. Its ability to participate in bromination, substitution, and other reactions can be harnessed to synthesize novel compounds with specific properties and applications.
Overall, 2,4-DibroModibenzo[b,d]furan-3-aMine is a versatile compound with diverse potential applications across different industries, including pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and properties make it an interesting target for research and development, offering opportunities for innovation and advancement in various scientific fields.

Check Digit Verification of cas no

The CAS Registry Mumber 133953-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,9,5 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 133953-35:
(8*1)+(7*3)+(6*3)+(5*9)+(4*5)+(3*3)+(2*3)+(1*5)=132
132 % 10 = 2
So 133953-35-2 is a valid CAS Registry Number.

133953-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dibromodibenzofuran-3-amine

1.2 Other means of identification

Product number -
Other names 3-Dibenzofuranamine,2,4-dibromo

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:133953-35-2 SDS

133953-35-2Relevant academic research and scientific papers

LUMINESCENT DIAZABENZIMIDAZOLE CARBENE METAL COMPLEXES

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Page/Page column 191; 192, (2015/02/25)

The present invention relates to metal-carbene complexes of the general formula (I), where variable M is Ir or Pt and that are characterized by variable R being a group of formula (a). The complexes are used in organic electronic devices, especially OLEDs (Organic Light-Emitting Diodes), illuminating elements, stationary visual display units and in material layers as emitter, charge transport material and/or charge or exiton blocker.

PHOSPHORESCENT EMITTERS

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, (2011/09/16)

Compounds including a ligand with a dibenzo-fused 5-membered ring substituent are provided. In particular, the compounds may be iridium complexes including imidazole coordinated to the dibenzo-substituted ligand. The dibenzo-fused 5-membered ring moiety of the ligand may be twisted or minimally twisted out of plane with respect to the rest of the ligand structure. The compound may be used in organic light emitting devices, particularly as emitting dopants in blue devices. Devices comprising the compounds may demonstrate improved stability while maintaining excellent color.

The synthesis and anti-MRSA activity of amidinium-substituted 2-dibenzofuranylcarbapenems

Laub, Joanne B.,Greenlee, Mark L.,DiNinno, Frank,Huber, Joann L.,Sundelof, Jon G.

, p. 2973 - 2976 (2007/10/03)

A series of amidinium-substituted 2-dibenzofuranylcarbapenems with potent activity against MRSA has been synthesized via a Stille cross-coupling reaction. These new carbapenems show reduced serum protein binding and improved in vivo efficacy as a conseque

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