Welcome to LookChem.com Sign In|Join Free

CAS

  • or

320-12-7

Post Buying Request

320-12-7 Suppliers

Recommended suppliersmore

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

320-12-7 Usage

Physical state

Colorless liquid

Odor

Slightly sweet

Common uses

Precursors in the synthesis of pharmaceuticals and fragrances, chiral auxiliary in organic synthesis

Safety precautions

Flammable, may cause skin and eye irritation upon contact

Check Digit Verification of cas no

The CAS Registry Mumber 320-12-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 320-12:
(5*3)+(4*2)+(3*0)+(2*1)+(1*2)=27
27 % 10 = 7
So 320-12-7 is a valid CAS Registry Number.

320-12-7SDS

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-(2'-fluorophenyl)propan-2-ol

1.2 Other means of identification

Product number -
Other names 2-(2-fluoro-phenyl)-propan-2-ol

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:320-12-7 SDS

320-12-7Relevant articles and documents

HETEROCYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

-

Paragraph 0512-0514, (2021/11/20)

Provided are a heterocyclic compound represented by Formula 1 and an organic light-emitting device including the same. The organic light-emitting device includes: a first electrode; a second electrode facing the first electrode; and an organic layer betwe

One-Pot C-H Arylation/Lactamization Cascade Reaction of Free Benzylamines

Chand-Thakuri, Pratibha,Landge, Vinod G.,Kapoor, Mohit,Young, Michael C.

supporting information, p. 6626 - 6644 (2020/07/14)

An efficient method has been developed for the synthesis of seven-membered biaryl lactams involving Pd-catalyzed, native amine-directed, ortho-arylation of benzylamines followed by in situ lactamization. This cascade sequence is enabled by the use of 2-iodobenzoates, which facilitates C-H arylation from the free amine under conditions that typically require an improved directing group approach. This reaction is characterized by a broad substrate scope with good functional group tolerance. The need for an ester versus carboxylic acid-functionalized coupling partner is also explored, as is the potential for synthesizing eight-membered biaryl lactams. Various applications are also investigated, including access to the aza-brassinolide core.

The cumene/O2 system: A very simple tool for the radical chain oxidation of some functional groups

Malekafzali,Malinovska,Patureau

supporting information, p. 6981 - 6985 (2017/08/02)

Due to the relative stability of the cumyl radical, cumenes and α-methyl-styrenes are ideally structured to directly harvest the oxidizing reactivity of O2 and initiate radical chain reactions in catalyst-free conditions. In the absence of additional substrates, these processes can lead to acetophenones. In the presence of substrates, the cumene oxidation process can be intercepted in various chain reactions, affording very simple protocols for functional group oxidation.

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

What can I do for you?
Get Best Price

Get Best Price for 320-12-7