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2 5-BIS(BROMOMETHYL)-1 4-BIS(3' 7'- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 129236-96-0 Structure
  • Basic information

    1. Product Name: 2 5-BIS(BROMOMETHYL)-1 4-BIS(3' 7'-
    2. Synonyms: 2 5-BIS(BROMOMETHYL)-1 4-BIS(3' 7'-
    3. CAS NO:129236-96-0
    4. Molecular Formula: C28H48Br2O2
    5. Molecular Weight: 576.48752
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 129236-96-0.mol
  • Chemical Properties

    1. Melting Point: 71-74 °C(lit.)
    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: 2 5-BIS(BROMOMETHYL)-1 4-BIS(3' 7'-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2 5-BIS(BROMOMETHYL)-1 4-BIS(3' 7'-(129236-96-0)
    11. EPA Substance Registry System: 2 5-BIS(BROMOMETHYL)-1 4-BIS(3' 7'-(129236-96-0)
  • Safety Data

    1. Hazard Codes: C
    2. Statements: 34
    3. Safety Statements: 26-36/37/39-45
    4. RIDADR: UN 1759 8/PG 2
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 129236-96-0(Hazardous Substances Data)

129236-96-0 Usage

Chemical compound

2,5-Bis(bromomethyl)-1,4-bis(3',7'-dibromo-2',6'-dihydroxyxanthene) is a chemical compound.

Used in synthesis

It is used in the synthesis of biologically active molecules and organic materials.

Dibromo derivative

It is a dibromo derivative of xanthene, a fluorescent dye used in biological staining and imaging.
溴甲基和二溴羟基蒽结构:The compound has two bromomethyl groups and two dibromo-2',6'-dihydroxyxanthene groups.

Cross-coupling reactions

It is suitable for cross-coupling reactions and other organic transformations.

Unique structure and reactivity

Its unique structure and reactivity make it a valuable building block for the synthesis of complex organic compounds and materials.

Potential applications

The compound has potential applications in medicine, biology, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 129236-96-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,2,3 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 129236-96:
(8*1)+(7*2)+(6*9)+(5*2)+(4*3)+(3*6)+(2*9)+(1*6)=140
140 % 10 = 0
So 129236-96-0 is a valid CAS Registry Number.

129236-96-0 Well-known Company Product Price

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  • Aldrich

  • (546496)  2,5-Bis(bromomethyl)-1,4-bis(3′,7′-dimethyloctyloxy)benzene  98%

  • 129236-96-0

  • 546496-1G

  • 2,726.10CNY

  • Detail

129236-96-0SDS

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 1,4-bis(bromomethyl)-2,5-bis(3,7-dimethyloctoxy)benzene

1.2 Other means of identification

Product number -
Other names -

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:129236-96-0 SDS

129236-96-0Relevant articles and documents

Isothermal and non-isothermal cold crystallization of tetrabenzofluorene (TBF) molecules

Boopathi,Sampath, Srinivasan,Narasimhaswamy

, p. 9500 - 9506 (2019/06/21)

Design and synthesis of tetrabenzo[a,c,g,i]fluorene (TBF) derivatives are carried out to investigate the isothermal and non-isothermal cold crystallization (CC) behavior by various spectroscopic and analytical techniques. The unprecedented CC exhibited by

Poly[(arylene ethynylene)-alt-(arylene vinylene)]s Based on Anthanthrone and Its Derivatives: Synthesis and Photophysical, Electrochemical, Electroluminescent, and Photovoltaic Properties

John, Suru Vivian,Cimrová, Věra,Ulbricht, Christoph,Pokorná, Veronika,Ru?i?ka, Ale?,Giguère, Jean-Benoit,Lafleur-Lambert, Antoine,Morin, Jean-Fran?ois,Iwuoha, Emmanuel,Egbe, Daniel Ayuk Mbi

, p. 8357 - 8371 (2017/11/21)

Anthanthrone and its derivatives are large polycyclic aromatic compounds (PACs) that pose a number of challenges for incorporation into the structure of soluble conjugated polymers. For the first time, this group of PACs was employed as the building blocks for the synthesis of copolymers (P1-P5) based on poly[(arylene ethynylene)-alt-(arylene vinylene)]s backbone (-Ph-C=C-Anth-C=C-Ph-CH - CH-Ph-CH - CH-)n. During the synthesis of P1-P5, different alkyloxy side chains were incorporated in order to tune the properties of the polymers. Of the copolymer series only P1 (containing anthanthrone and branched 2-ethylhexyloxy side chains on phenylenes), P2 and P3 (for which the anthanthrones containing carbonyl groups were converted to anthanthrene containing alkyloxy substituents) were soluble. The photophysical, electrochemical, electroluminescent and photovoltaic properties of P1-P3 are reported, compared and discussed with respect to the effects of side chains.

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