16868-13-6

• 

• Basic information

  1. Product Name: CYCLOPENTYL ACRYLATE
  2. Synonyms: 2-propenoicacid,cyclopentylester;CYCLOPENTYL ACRYLATE;ACRYLICACID,CYCLOPENTYLESTER;Propenoic acid cyclopentyl ester;Einecs 240-889-4
  3. CAS NO:16868-13-6
  4. Molecular Formula: C₈H₁₂O₂
  5. Molecular Weight: 140.18
  6. EINECS: 240-889-4
  7. Product Categories: monomer
  8. Mol File: 16868-13-6.mol
  9. Article Data: 3

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 175.8°Cat760mmHg
  3. Flash Point: 58.4°C
  4. Appearance: /
  5. Density: 0.99g/cm³
  6. Vapor Pressure: 1.13mmHg at 25°C
  7. Refractive Index: 1.458
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: CYCLOPENTYL ACRYLATE(CAS DataBase Reference)
  11. NIST Chemistry Reference: CYCLOPENTYL ACRYLATE(16868-13-6)
  12. EPA Substance Registry System: CYCLOPENTYL ACRYLATE(16868-13-6)

• 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: 16868-13-6(Hazardous Substances Data)

• Suppliers
• Usage
• SDS
• Upstream product
• Downstream Products
• Article

16868-13-6 Suppliers

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• Cyclopentyl acrylate

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• Dayang Chem (Hangzhou) Co.,Ltd.
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• 2-Propenoic acid,cyclopentyl ester

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• 10 Gram

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• Zibo Hangyu Biotechnology Development Co., Ltd
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• 2-Propenoic acid,cyclopentyl ester

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• CYCLOPENTYL ACRYLATE

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• 2-Propenoic acid,cyclopentyl ester

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• Cyclopentyl acrylate

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16868-13-6 Usage

General Description

Cyclopentyl acrylate is a chemical compound with the molecular formula C8H12O2. It is a clear, colorless liquid that is used in the production of polymers and other industrial applications. Cyclopentyl acrylate is a type of acrylate monomer, which means it contains a vinyl group and a carboxyl group, making it suitable for use in polymerization reactions. It is commonly used in the manufacture of adhesives, coatings, and resins, and is known for its excellent adhesion and resistance properties. This chemical is also used in the production of specialty polymers for various industrial applications. However, it should be handled with care and stored properly due to its potential health and safety hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 16868-13-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,6 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16868-13:
(7*1)+(6*6)+(5*8)+(4*6)+(3*8)+(2*1)+(1*3)=136
136 % 10 = 6
So 16868-13-6 is a valid CAS Registry Number.

InChI:InChI=1/C8H12O2/c1-2-8(9)10-7-5-3-4-6-7/h2,7H,1,3-6H2

16868-13-6SDS

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	cyclopentyl prop-2-enoate

1.2 Other means of identification

Product number	-
Other names	Cyclopentyl-acrylat

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:16868-13-6 SDS

16868-13-6Upstream product

• 96-41-3 Cyclopentanol 
• 79-10-7 acrylic acid 
• 50706-57-5 4-(diphenylmethylene)piperidine 
• 106-63-8 isobutyl acrylate 
• 142-29-0 cyclopentene 
• 814-68-6 acryloyl chloride 

16868-13-6Downstream Products

16868-13-6Relevant articles and documents

Asymmetric Diels-Alder reaction between acrylates and cyclopentadiene in the presence of chiral catalysts

Mamedov

, p. 1621 - 1625 (2008/02/07)

Asymmetric Diels-Alder reaction between cyclopentadiene and alkyl and cycloalkyl acrylates in the presence of new chiral catalysts, BBr 3?MentOEt, AlCl2OMent, BBr2OMent, and BBr(OMent)2, was studied. Optically active bicyclo[2.2.1]hept-2-ene- 5-carboxylates were synthesized. The influence of the reaction conditions on the total and optical yields and on the stereoselectivity of the adducts synthesized was examined. Nauka/Interperiodica 2006.

TREATMENT OF CNS DISORDERS USING CNS TARGET MODULATORS

-

, (2008/06/13)

The invention is directed to compositions used for treating Central Nervous System (CNS) disorders. In addition, the invention provides convenient methods of treatment of a CNS disorder. Furthermore, the invention provides methods of treating sleep disorders using compositions that remain active for a discrete period of time to reduce side effects. More specifically, the invention is directed to the compositions and use of derivatized, e.g., ester or carboxylic acid derivatized, antihistamine antagonists for the treatment of sleep disorders.

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