Welcome to LookChem.com Sign In|Join Free
  • or
Naphthalene, 2-bromo-1-(2-propenyloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

848780-28-9

Post Buying Request

848780-28-9 Suppliers

Recommended suppliers

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

848780-28-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 848780-28-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,7,8 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 848780-28:
(8*8)+(7*4)+(6*8)+(5*7)+(4*8)+(3*0)+(2*2)+(1*8)=219
219 % 10 = 9
So 848780-28-9 is a valid CAS Registry Number.

848780-28-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-1-prop-2-enoxynaphthalene

1.2 Other means of identification

Product number -
Other names 1-allyloxy-2-bromo-naphthalene

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:848780-28-9 SDS

848780-28-9Downstream Products

848780-28-9Relevant academic research and scientific papers

An approach to the synthesis of naphtho[b]furans from allyl bromonaphthyl ethers employing sequential photoinduced radical cyclization and dehydrohalogenation reactions

Suzuki, Yusuke,Okita, Yoshiki,Morita, Toshio,Yoshimi, Yasuharu

supporting information, p. 3355 - 3357 (2014/06/09)

A simple method has been developed for the efficient synthesis of naphtho[b]furans from allyl bromonaphthyl ethers. The approach utilizes a novel photochemical process involving sequential radical cyclization and dehydrohalogenation. Because light is a readily available, environmentally friendly reagent that produces no by-products, the new process serves as a green synthetic method.

Synthesis and biological evaluation of (±)-cryptotanshinone and its simplified analogues as potent CDC25 inhibitors

Huang, Wei Gang,Jiang, Ying Yan,Li, Qian,Li, Jia,Li, Jing Ya,Lu, Wei,Cai, Jun Chao

, p. 1863 - 1870 (2007/10/03)

(±)-Cryptotanshinone and its simplified analogues were synthesized via SmI2 promoted radical cyclization to construct the furan ring. Analogues 18 and 26 were identified as effective inhibitors of dual specificity protein phosphatase CDC25B which is a key enzyme for cell cycle progression, and they also inhibited growth in A-549 human lung cancer cell line.

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 848780-28-9