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  • 53076-11-2 Structure
  • Basic information

    1. Product Name: 4-Hydroxymethylbenzocyclobutene
    2. Synonyms: 4-hydroxymethylbenzocyclobutene;4-HYDROXYBENZOCYCLOBUTENE;Bicyclo[4.2.0]octa-1,3,5,7-tetraen-3-ylMethanol;4-HMBCB 4-hydroxymethylbenzocyclobutene;4-bicyclo[4.2.0]octa-1(6),2,4-trienylmethanol
    3. CAS NO:53076-11-2
    4. Molecular Formula: C9H8O
    5. Molecular Weight: 132.16
    6. EINECS: N/A
    7. Product Categories: API intermediates
    8. Mol File: 53076-11-2.mol
    9. Article Data: 2
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 266.319°C at 760 mmHg
    3. Flash Point: 130.67°C
    4. Appearance: /
    5. Density: 1.171g/cm3
    6. Vapor Pressure: 0.004mmHg at 25°C
    7. Refractive Index: 1.62
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: 14.50±0.10(Predicted)
    11. CAS DataBase Reference: 4-Hydroxymethylbenzocyclobutene(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-Hydroxymethylbenzocyclobutene(53076-11-2)
    13. EPA Substance Registry System: 4-Hydroxymethylbenzocyclobutene(53076-11-2)
  • 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: 53076-11-2(Hazardous Substances Data)

53076-11-2 Usage

Description

4-Hydroxymethylbenzocyclobutene, a bicyclic organic compound with the molecular formula C9H10O, is a type of benzocyclobutene characterized by the fusion of a benzene ring with a cyclobutene ring. Derived from benzocyclobutene, this compound features a hydroxymethyl group attached to the benzene ring, which endows it with diverse applications in various industries.

Uses

Used in Chemical Synthesis:
4-Hydroxymethylbenzocyclobutene is utilized as a building block in the synthesis of other organic compounds, contributing to the creation of a wide range of chemical products.
Used in Polymer Production:
4-Hydroxymethylbenzocyclobutene also serves as a component in the production of polymers, where its unique structure and properties enhance the characteristics of the resulting polymeric materials.
Used in Pharmaceutical and Medicinal Research:
4-Hydroxymethylbenzocyclobutene has been studied for its potential pharmaceutical and medicinal uses, indicating its value in the development of new drugs and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 53076-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,0,7 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53076-11:
(7*5)+(6*3)+(5*0)+(4*7)+(3*6)+(2*1)+(1*1)=102
102 % 10 = 2
So 53076-11-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O/c10-6-7-1-2-8-3-4-9(8)5-7/h1-2,5,10H,3-4,6H2

53076-11-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bicyclo[4.2.0]octa-1(6),2,4,7-tetraenylmethanol

1.2 Other means of identification

Product number -
Other names 4-hydroxymethylbenzocyclobutene

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:53076-11-2 SDS

53076-11-2Downstream Products

53076-11-2Relevant articles and documents

Synthesis of optically active benzocyclobutene and biphenylene based unusual α-amino acid derivatives

Kotha, Sambasivarao,Halder, Somnath

, p. 863 - 872 (2007/10/03)

Optically active benzocyclobutene and biphenylene based unusual α-amino acid derivatives have been prepared via a six step sequence using Schoellkopf chiral auxiliary in a very high diastereoselective manner.

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