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86717-90-0

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86717-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86717-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,1 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86717-90:
(7*8)+(6*6)+(5*7)+(4*1)+(3*7)+(2*9)+(1*0)=170
170 % 10 = 0
So 86717-90-0 is a valid CAS Registry Number.

86717-90-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-bromopropoxy)acetophenone

1.2 Other means of identification

Product number -
Other names 1[2-(3-bromopropoxy)phenyl]ethanone

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:86717-90-0 SDS

86717-90-0Relevant articles and documents

Demonstration of 11-21-Membered Intramolecular Sulfonium Ylides: Regio- and Diastereoselective Synthesis of Spiro-Oxindole-Incorporated Macrocycles

Muthusamy, Sengodagounder,Selvaraj, Karuppu,Suresh, Eringathodi

, p. 1849 - 1859 (2016/04/20)

An expeditious and convenient method for the generation of 11-21-membered intramolecular macrocyclic sulfonium ylides using catalytic Rh2(OAc)4 is presented. Using this approach, a wide variety of sulfur-macrocycles incorporating the

Cyclization of 2-(2-bromoethoxy)-acetophenones and 5-(ω-haloalkoxy)- 1,5-dihydro-2H-pyrrol-2-ones - Formation of five- to eight-membered oxygen-containing heterocycles via intramolecular alkylation

Nikitin, Kirill V.,Andryukhova, Nonna P.

, p. 571 - 578 (2007/10/03)

Under basic conditions (lithium diisopropylamide or sodium hydride in THF) 2-(2-bromoethoxy)-acetophenones were transformed to 3,4-dihydro[1]benzoxepin- 5(2H)-ones (homochromanones) in high yields. The preparation of novel tetrahydropyrano[2,3-b]pyrrol-6(

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