Welcome to LookChem.com Sign In|Join Free
  • or
1(2H)-Naphthalenone, 3,4-dihydro-6,7-bis(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119034-87-6

Post Buying Request

119034-87-6 Suppliers

Recommended suppliers

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

119034-87-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119034-87-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,0,3 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 119034-87:
(8*1)+(7*1)+(6*9)+(5*0)+(4*3)+(3*4)+(2*8)+(1*7)=116
116 % 10 = 6
So 119034-87-6 is a valid CAS Registry Number.

119034-87-6SDS

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 6,7-bis(phenylmethoxy)-3,4-dihydro-2H-naphthalen-1-one

1.2 Other means of identification

Product number -
Other names 6,7-dibenzyloxy-1-tetralone

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:119034-87-6 SDS

119034-87-6Relevant academic research and scientific papers

BETA-2 SELECTIVE ADRENERGIC RECEPTOR AGONISTS

-

Page/Page column 77-78, (2019/06/23)

Aspects of the present disclosure include conformationally restricted analogs of catecholamine type compounds (e.g., isoprenaline, adrenaline, noradrenaline) which activate β2AR with high selectivity over β1AR. The subject beta-2 selective adrenergic rece

Catalytic asymmetric synthesis of halenaquinone and halenaquinol

Kojima,Takemoto,Sodeoka,Shibasaki

, p. 581 - 589 (2007/10/03)

A catalytic asymmetric synthesis of halenaquinone (1) and halenaquinol (2) has been achieved using an asymmetric Heck reaction or a cascade Suzuki cross-coupling and an asymmetric Heck reaction as a key step. This synthesis also features the one-pot construction of a unique pentacyclic ring system from a tricyclic system using palladium chemistry. Moreover, the use of Ph3As as an achiral ligand has been found to enhance both the cascade Suzuki cross-coupling and also the Heck reaction to a synthetically useful extent.

Hexahydronaphth[1,2-b]-1,4-oxazines

-

, (2008/06/13)

Hexahydronaphth[1,2-b]-1,4-oxazines have dopaminergic activity and display α 2 -adrenergic receptor antagonism. They are useful in the treatment of parkinsonism, depression and hypertension. An important method of preparation is by ring closure of the app

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 119034-87-6