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1159977-09-9

rac Benzyl Phenylephrine (Phenylephrine Impurity D) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1159977-09-9

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1159977-09-9 Usage

Chemical Properties

Pale Yellow Waxy Solid

Uses

Impurity D of Phenylephrine.

Check Digit Verification of cas no

The CAS Registry Mumber 1159977-09-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,9,9,7 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1159977-09:
(9*1)+(8*1)+(7*5)+(6*9)+(5*9)+(4*7)+(3*7)+(2*0)+(1*9)=209
209 % 10 = 9
So 1159977-09-9 is a valid CAS Registry Number.

1159977-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name rac Benzyl Phenylephrine

1.2 Other means of identification

Product number -
Other names 3-[2-[benzyl(methyl)amino]-1-hydroxyethyl]phenol

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:1159977-09-9 SDS

1159977-09-9Downstream Products

1159977-09-9Relevant articles and documents

Method for Ir/f-amphox high-efficiency synthesis of chiral α- C-amino alcohol by virtue of catalytic oxidation 1,2- of P-aminoketone by using one-aminoketone

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Paragraph 0073-0078, (2020/01/03)

The invention discloses a method for efficiently synthesizing chiral 1,2-amino alcohol by catalyzing alpha-aminoketone through Ir/f-amphox. A ligand f-amphox used by the method can be more easily synthesized; the reaction has the characteristics of enanti

Method for preparing of L-phenylephrine hydrochloride

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, (2008/06/13)

The present invention relates to an improved process for preparing L-phenylephrine hydrochloride 3 on an industrial scale by asymmetric hydrogenation as the key step and a special sequence of subsequent steps, using [Rh(COD)Cl]2 as catalyst and a chiral, two-pronged phosphine ligand such as (2R,4R)-4-(dicyclohexylphosphino)-2-(diphenylphosphino-methyl)-N-methyl-aminocarbonyl-pyrrolidine as the catalyst system.

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