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Benzoesure, 4-[[6-[(1-oxo-2-propenyl)oxy]hexyl]oxy]-, 4-methoxyphenylester is a complex chemical compound that consists of multiple components. It is derived from benzoic acid (Benzoesure), with additional elements including propenyl (1-oxo-2-propenyl), a hexyl (six-carbon chain), and a methoxyphenyl ester. The presence of "oxy" and "ester" in its name indicates the inclusion of oxygen-containing groups and ester linkages within its molecular structure. The specific properties, applications, reactivity, toxicity, and pharmacological effects of this compound would be determined by the precise arrangement and bonding of these components, necessitating a detailed chemical analysis or research studies for a comprehensive understanding.

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  • 4-[[6-[(1-Oxo-2-propenyl)oxy]hexyl]oxy]benzoic acid 4-Methoxyphenyl ester

    Cas No: 82200-53-1

  • USD $ 1.9-2.9 / Gram

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  • 82200-53-1 Structure
  • Basic information

    1. Product Name: Benzoesure, 4-[[6-[(1-oxo-2-propenyl)oxy]hexyl]oxy]-, 4-methoxyphenylester
    2. Synonyms: Benzoesure, 4-[[6-[(1-oxo-2-propenyl)oxy]hexyl]oxy]-, 4-methoxyphenylester;4-Methoxyphenyl-4-(6-(acryloyloxy)hexyloxy)benzoate;4-[[6-[(1-Oxo-2-propenyl)oxy]hexyl]oxy]benzoic acid 4-Methoxyphenyl ester;Benzoic acid,4-[[6-[(1-oxo-2-propen-1-yl)oxy]hexyl]oxy]-, 4-Methoxyphenyl ester
    3. CAS NO:82200-53-1
    4. Molecular Formula: C23H26O6
    5. Molecular Weight: 398.44894
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82200-53-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 539.9±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.133±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzoesure, 4-[[6-[(1-oxo-2-propenyl)oxy]hexyl]oxy]-, 4-methoxyphenylester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoesure, 4-[[6-[(1-oxo-2-propenyl)oxy]hexyl]oxy]-, 4-methoxyphenylester(82200-53-1)
    11. EPA Substance Registry System: Benzoesure, 4-[[6-[(1-oxo-2-propenyl)oxy]hexyl]oxy]-, 4-methoxyphenylester(82200-53-1)
  • 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: 82200-53-1(Hazardous Substances Data)

82200-53-1 Usage

Uses

Since the provided materials do not explicitly list the uses of Benzoesure, 4-[[6-[(1-oxo-2-propenyl)oxy]hexyl]oxy]-, 4-methoxyphenylester, it is not possible to provide a detailed list of applications based on the information given. However, given the complexity of its structure, it is likely that this compound could have potential applications in various fields such as pharmaceuticals, chemical research, or material science, similar to other complex organic compounds. Further research and analysis would be required to determine its specific uses and benefits in these or other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 82200-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,0 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82200-53:
(7*8)+(6*2)+(5*2)+(4*0)+(3*0)+(2*5)+(1*3)=91
91 % 10 = 1
So 82200-53-1 is a valid CAS Registry Number.

82200-53-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(6-acryloyloxyhexyloxy)benzoic acid 4-methoxyphenyl ester

1.2 Other means of identification

Product number -
Other names 4-METHOXYPHENYL-4-(6-(ACRYLOYLOXY)HEXYLOXY)BENZOATE

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:82200-53-1 SDS

82200-53-1Downstream Products

82200-53-1Relevant articles and documents

Allyl sulfide-based visible light-induced dynamically reshaped liquid crystalline elastomer/SWCNT nanocomposites capable of multimode NIR photomechanical actuations

Chen, Dongzhong,Cheng, Pin,Fang, Jianglin,Wu, Zhongying,Xu, Tianchi,Zhao, Weiguang

supporting information, p. 10902 - 10910 (2020/07/15)

Liquid crystalline elastomers (LCEs) combine the ordering character of a liquid crystal and the elasticity of a polymer network. The development of fully light-driven LCE-based soft actuators with good reshapeability and recyclability is in high demand. In this work, we prepared SWCNT/LCE composite films through the introduction of allyl sulfide-based dynamic covalent crosslinks in the LCE matrix and the well-dispersed filler single-walled carbon nanotubes (SWCNTs) with a strong photothermal effect. The SWCNT/LCE composite films were facilely fabricated with reorientation and remouldable capabilities regulated by 405 nm visible light. The monodomain composite films demonstrated multimode actuations of contraction, bending, curling, stretching recovery, and even shape memory driven by 808 nm near-infrared (NIR) light. Moreover, the monodomain spiral ribbon or stretching flat strip and the original polydomain composite film can be readily transformed into each other, and reshaped through easily achievable fabrication conditions. Therefore, the well-prepared SWCNT/LCE composite films with exchangeable covalent crosslinks showed promise as candidates for the development of multimode NIR photomechanical soft actuators with fully light-driven controllability and good remouldability. This journal is

POLYMERIZABLE COMPOUND AND COMPOSITION CONTAINING THE POLYMERIZABLE COMPOUND

-

Page/Page column 37-38, (2010/11/28)

The polymerizable compound of the present invention is represented by general formula (1) below and can provide a composition that is polymerizable near ambient temperature and exists in a liquid crystal phase at low temperatures. The composition and a (co)polymer of the polymerizable compound of the present invention are liquid crystal substances useful as optically anisotropic materials. (In the formula, each of rings A1 to A3 represents a benzene ring, cyclohexane ring, etc.; each of X to Z represents a C1-8 alkyl or alkoxy group, C2-6 alkenyl group, halogen atom, cyano group, or CH2=CR3-COO-; each of R1 to R3 represents a hydrogen atom, methyl group, or halogen atom; each of L1 to L3 represents -CH2CH2COO-, -COO-, -OCO-, -CH2CH2-, -O(CH2)f- (herein, f = 1-8), etc.; n represents 0 or 1; and a to c represent such numbers that the polymerizable compound has at least one or more of any of X, Y, and Z.)

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