Welcome to LookChem.com Sign In|Join Free
  • or
4-16-00-01011 (Beilstein Handbook Reference) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90177-29-0

Post Buying Request

90177-29-0 Suppliers

Recommended suppliers

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

90177-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90177-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,7 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90177-29:
(7*9)+(6*0)+(5*1)+(4*7)+(3*7)+(2*2)+(1*9)=130
130 % 10 = 0
So 90177-29-0 is a valid CAS Registry Number.

90177-29-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name n-dodecyl-diphenylphosphine oxide

1.2 Other means of identification

Product number -
Other names dodecyl-diphenyl-phosphine oxide

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:90177-29-0 SDS

90177-29-0Downstream Products

90177-29-0Relevant academic research and scientific papers

Palladium-catalyzed C(sp3)–P(III) bond formation reaction with acylphosphines as phosphorus source

Zhang, Mengyue,Ma, Zhichao,Du, Hongguang,Wang, Zhiqian

, (2020/06/29)

Palladium-catalyzed C(sp3)–P(III) bond formation reaction for alkyl substituted phosphines preparation was developed. In this reaction, various alkyl bromides and limited alkyl chlorides reacted with acylphosphine under relative mild and easily accessible condition, and differential phosphines were afforded in good yields. This reaction made up the application of palladium catalysis in C(sp3)–P(III) bond formation, and indicated a practical application of acylphosphine as a phosphination reagent.

Et3B-induced radical addition of diphenylphosphine oxide to unsaturated compounds

Rey, Patrick,Taillades, Jacques,Rossi, Jean Christophe,Gros, Georges

, p. 6169 - 6171 (2007/10/03)

Et3B-catalysed addition of diphenylphosphine oxide to unsaturated compounds, alkenes, unsaturated acids, allylic alcohols, and allylic α-O-acetyl nitriles constitutes a practical route to a variety of functionalized diphenylphosphine oxides. Th

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 90177-29-0