156492-30-7

• 

• Basic information

  1. Product Name: 1,10-Phenanthroline, 4,7-dibroMo-
  2. Synonyms: 1,10-Phenanthroline, 4,7-dibroMo-;4,7-DibroMophenanthroline;4,7-Dibromo-1,10-phenanthroline Hydrate;1,10-Phenthroline, 4,7-dibroMo-
  3. CAS NO:156492-30-7
  4. Molecular Formula: C₁₂H₆Br₂N₂
  5. Molecular Weight: 337.99744
  6. EINECS: 1592732-453-0
  7. Product Categories: N/A
  8. Mol File: 156492-30-7.mol
  9. Article Data: 6

• Chemical Properties

  1. Melting Point: 236℃
  2. Boiling Point: 466.6±40.0 °C(Predicted)
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 1.915±0.06 g/cm3(Predicted)
  6. Refractive Index: N/A
  7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
  8. Solubility: N/A
  9. PKA: 3.29±0.10(Predicted)
  10. CAS DataBase Reference: 1,10-Phenanthroline, 4,7-dibroMo-(CAS DataBase Reference)
  11. NIST Chemistry Reference: 1,10-Phenanthroline, 4,7-dibroMo-(156492-30-7)
  12. EPA Substance Registry System: 1,10-Phenanthroline, 4,7-dibroMo-(156492-30-7)

• 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: 156492-30-7(Hazardous Substances Data)

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• 4,7-Dibromo-1,10-phenanthroline

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156492-30-7 Usage

General Description

1,10-Phenanthroline, 4,7-dibromo- is a chemical compound with the molecular formula C12H6Br2N2. It is an asymmetrical bidentate chelating ligand commonly used in coordination chemistry. 1,10-Phenanthroline, 4,7-dibromo- is known for its fluorescent properties and is often used as a reagent in analytical chemistry, particularly in the determination of metal ions. It has also been studied for its potential application in pharmaceuticals, as it has been found to exhibit antimicrobial and antiparasitic properties. Overall, 1,10-Phenanthroline, 4,7-dibromo- is a versatile chemical compound with various applications in the field of chemistry and biology.

Check Digit Verification of cas no

The CAS Registry Mumber 156492-30-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,4,9 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 156492-30:
(8*1)+(7*5)+(6*6)+(5*4)+(4*9)+(3*2)+(2*3)+(1*0)=147
147 % 10 = 7
So 156492-30-7 is a valid CAS Registry Number.

156492-30-7 Well-known Company Product Price

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• TCI America

• (D4987)  4,7-Dibromo-1,10-phenanthroline Hydrate  >98.0%(HPLC)

• 156492-30-7

• 200mg

• 890.00CNY

• Detail

• TCI America

• (D4987)  4,7-Dibromo-1,10-phenanthroline Hydrate  >98.0%(HPLC)

• 156492-30-7

• 1g

• 3,200.00CNY

• Detail

156492-30-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name	4,7-dibromo-1,10-phenanthroline

1.2 Other means of identification

Product number	-
Other names	4,7-Dibrom-[1,10]phenanthrolin

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:156492-30-7 SDS

156492-30-7Upstream product

• 87330-27-6 1,4,7,10-tetrahydro-1,10-phenanthroline-4,7-dione 
• 95-54-5 1,2-diamino-benzene 
• 3922-40-5 1,10-phenanthroline-4,7-diol 
• 2033-24-1 cycl-isopropylidene malonate 
• 503863-91-0 1,2-bis-[(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ylidenemethyl)amino]benzene 

156492-30-7Downstream Products

• 7089-67-0 4-bromo-1,10-phenanthroline 
• 97802-07-8 4-p-bromophenyl-1,10-phenanthroline 
• 959625-99-1 C₈₀H₉₆N₂O₄ 
• 192226-55-4 4,7-bis(phenylethinyl)-1,10-phenanthroline 

156492-30-7Relevant articles and documents

Bright and Long-Lived Emission from a Starburst-Type Arylborane-Appended Polypyridyl Ruthenium(II) Complex

Nakagawa, Atsushi,Ito, Akitaka,Sakuda, Eri,Fujii, Sho,Kitamura, Noboru

, p. 3794 - 3798 (2017)

The starburst-type arylborane-appended polypyridyl RuII complex [Ru{4,7-bis({dimesityl}boryldurylethynyl)-1,10-phenanthroline}3]2+ (1) was synthesized, and its spectroscopic and photophysical properties were evaluated. In the excited state of the complex, intramolecular charge transfer (CT) between the π orbital of the aryl group and the vacant p orbital of the boron atom [π(aryl)–p(B) CT] interacts synergistically with metal-to-ligand charge transfer (MLCT). The synergistic CT interactions in 1 are more effective than those in previously reported arylborane-appended polypyridyl RuII complexes and lead to bright (molar absorption coefficient of the MLCT band = 7.2 × 104 m–1 cm–1, emission quantum yield = 0.29) and long-lived emission (8.7 μs) of 1 in CH3CN at 298 K. The unique emission characteristics of 1 are discussed in detail together with its electrochemical properties and time-dependent DFT (TD-DFT) calculations.

Organic electroluminescence material and organic photoelectric device

-

Paragraph 0129; 0134; 0135, (2017/07/19)

The invention provides a compound with a structure as shown in formula I. The invention also provides an application of the compound in an organic photoelectric device and the organic photoelectric device. The compound provided by the invention has a ther

The synthesis of aromatic diazatricycles from phenylenediamine-bis(methylene Meldrum's acid) derivatives

Graf, Gabriele Ina,Hastreiter, Daniel,Da Silva, Luiz Everson,Rebelo, Ricardo Andrade,Montalban, Antonio Garrido,McKillop, Alexander

, p. 9095 - 9100 (2007/10/03)

The thermocyclisation of phenylenediamine-bis(methylene Meldrum's acid) derivatives has been investigated. Those of o-phenylenediamines give 1,10-phenanthroline derivatives, while those of m- and p-phenylenediamines lead to the preferential formation of angular diazatricycles. Thus, for example, the di-Meldrum's acid derivative of 2,5-dichloro-1,4-phenylenediamine gives, via ipso-substitution, the unexpected angular product 19.

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