Welcome to LookChem.com Sign In|Join Free
  • or
3-Hexyn-2-ol, 6-(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89121-83-5

Post Buying Request

89121-83-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

89121-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89121-83-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,2 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89121-83:
(7*8)+(6*9)+(5*1)+(4*2)+(3*1)+(2*8)+(1*3)=145
145 % 10 = 5
So 89121-83-5 is a valid CAS Registry Number.

89121-83-5SDS

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 6-phenylmethoxyhex-3-yn-2-ol

1.2 Other means of identification

Product number -
Other names 3-Hexyn-2-ol,6-(phenylmethoxy)

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:89121-83-5 SDS

89121-83-5Relevant academic research and scientific papers

Synthesis of dienol ethers using the phosphine-catalyzed alkyne isomerization reaction

Fu, Michael Yunyi,Guo, Jiawen,Toy, Patrick H.

scheme or table, p. 989 - 991 (2011/06/17)

A series of -alkoxy-substituted electron-deficient alkynes were isomerized to the corresponding dienol ethers using phosphine catalysis. Both Ph 3P and a polymer-supported phosphine were found to be useful in this context. This methodology represents a general procedure for the synthesis of push-pull' -alkoxy dienones. Georg Thieme Verlag Stuttgart · New York.

Secondary allyltitanium(IV) reagents in aldehyde allylation I: Extension of the Hoppe reaction to γ-alkoxy secondary allyl carbamates

Razon, Patrick,Dhulut, Sylvie,Bezzenine-Lafollee, Sophie,Courtieu, Jacques,Pancrazi, Ange,Ardisson, Janick

, p. 102 - 108 (2007/10/03)

An efficient access to optically active (R)- or (S)-γ-alkoxy allyltitanium(IV) intermediates, in aldehyde allylation reactions, is described. Enantiomeric γ-alkoxy secondary allyl carbamates (R)- and (S)-14 were first prepared. Determination of their enan

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 89121-83-5