121983-06-0

• 

• Basic information

  1. Product Name: Cyclopentane, 1-ethynyl-1-(2-propenyloxy)- (9CI)
  2. Synonyms: Cyclopentane, 1-ethynyl-1-(2-propenyloxy)- (9CI)
  3. CAS NO:121983-06-0
  4. Molecular Formula: C₁₀H₁₄O
  5. Molecular Weight: 150.21756
  6. EINECS: N/A
  7. Product Categories: METHOXY
  8. Mol File: 121983-06-0.mol
  9. Article Data: 4

• Chemical Properties

  1. Melting Point: N/A
  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: Cyclopentane, 1-ethynyl-1-(2-propenyloxy)- (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Cyclopentane, 1-ethynyl-1-(2-propenyloxy)- (9CI)(121983-06-0)
  11. EPA Substance Registry System: Cyclopentane, 1-ethynyl-1-(2-propenyloxy)- (9CI)(121983-06-0)

• 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: 121983-06-0(Hazardous Substances Data)

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

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121983-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121983-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,9,8 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 121983-06:
(8*1)+(7*2)+(6*1)+(5*9)+(4*8)+(3*3)+(2*0)+(1*6)=120
120 % 10 = 0
So 121983-06-0 is a valid CAS Registry Number.

121983-06-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	1-(allylloxy)-1-ethynylcyclopentane

1.2 Other means of identification

Product number	-
Other names	1-Allyloxy-1-ethynyl-cyclopentane

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:121983-06-0 SDS

121983-06-0Upstream product

• 71321-24-9 1-<2-(Trimethylsilyl)ethynyl>cyclopentan-1-ol 
• 120-92-3 cyclopentanone 
• 17356-19-3 1-ethynylcyclopentanol 
• 106-95-6 allyl bromide 

121983-06-0Downstream Products

121983-06-0Relevant articles and documents

INTRAMOLECULAR CYCLIZATION OF DICOBALT HAXACARBONYL COMPLEXES OF ALLYL PROPYL ETHERS ON ADSORBENT SURFACES. A CONVENIENT MODE OF PREPARATION OF 3-OXABICYCLOOCTENES AND 4-HYDROXYMETHYLCYCLOPENTENONE DERIVATIVES

Smit, V. A.,Simonyan, S. O.,Tarasov, V. A.,Gybin, A. S.,Mikaelyan, G. S.,et al.

, p. 2526 - 2535 (1988)

-

Ethylene-promoted versus ethylene-free enyne metathesis

Grotevendt, Anne G. D.,Lummiss, Justin A. M.,Mastronardi, Melanie L.,Fogg, Deryn E.

supporting information; experimental part, p. 15918 - 15921 (2011/11/13)

The role of ethylene in promoting metathesis of acetylenic enynes is probed within the context of ring-closing enyne metathesis, using first- and second-generation Grubbs catalysts. Under inert atmosphere, rapid catalyst deactivation is observed by calibr

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