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19343-24-9

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19343-24-9 Usage

Chemical class

Alcohol

Contains groups

Benzyl group, isopropylamino group, and propanol group

Common use

Starting material in organic synthesis and as a reagent in chemical reactions

Applications

Pharmaceutical industry (synthesis of drugs and pharmaceutical intermediates)

Potential applications

Organic chemistry and as a building block for more complex compounds

Physiological properties

May exhibit properties and act as a pharmacologically active compound

Versatility

Diverse applications in various industries
This list provides a concise overview of the key characteristics and uses of 1-(Benzyloxy)-3-(isopropylamino)-2-propanol, based on the information provided.

Check Digit Verification of cas no

The CAS Registry Mumber 19343-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,4 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19343-24:
(7*1)+(6*9)+(5*3)+(4*4)+(3*3)+(2*2)+(1*4)=109
109 % 10 = 9
So 19343-24-9 is a valid CAS Registry Number.

19343-24-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenylmethoxy-3-(propan-2-ylamino)propan-2-ol

1.2 Other means of identification

Product number -
Other names F0050-0006

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:19343-24-9 SDS

19343-24-9Downstream Products

19343-24-9Relevant articles and documents

Nucleophilic Addition to Cyclic 1,2-Sulfites

Carlsen, Per H.,Aase, Kristin J.

, p. 617 - 619 (2007/10/02)

Addition of heteroatom nucleophiles has been shown to attack at either the C5- or the S-atom sites in 4-(benzyloxymethyl)-1,3-dioxa-2-thiolane 2-oxide.No C4-reactivity was observed.The regioselectivity depended on the type of nucleophile.

Dihydro azino isoquinolines

-

, (2008/06/13)

The invention provides novel 1,5-substituted isoquinoline derivatives of formula I which are useful in the treatment of hypertension.

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