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1701-77-5

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1701-77-5 Usage

General Description

Methoxy(phenyl)acetic acid is a chemical compound with the molecular formula C9H10O3. It is an organic compound with a methoxy group (CH3O) attached to the benzene ring and an acetic acid group (-COOH) at the para position. methoxy(phenyl)acetic acid is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. It is also used as a reagent in organic chemistry reactions, particularly in the formation of esters and amides. Methoxy(phenyl)acetic acid is a white crystalline solid with a faint odor, and it is soluble in common organic solvents like ethanol and ether. It is important to handle this compound with care, as it is irritant to the skin, eyes, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 1701-77-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,0 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1701-77:
(6*1)+(5*7)+(4*0)+(3*1)+(2*7)+(1*7)=65
65 % 10 = 5
So 1701-77-5 is a valid CAS Registry Number.

1701-77-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name .α.-Methoxyphenylacetic acid

1.2 Other means of identification

Product number -
Other names -

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:1701-77-5 SDS

1701-77-5Relevant articles and documents

Resolution of (±)-mandelic- and (±)-2-(chiorophenoxy)propionic-acid derivatives by crystallization of their diastereomeric amides with (R)- or (S)-α-arylethylamines

Jourdain, Franck,Hirokawa, Takahiko,Kogane, Tamizo

, p. 2509 - 2512 (2007/10/03)

An alternative and cost effective route for the resolution in high ees (95-99%) of (±)-mandelic-and (±)-2-(chlorophenoxy)propionic- acid derivatives is reported. The key step involves the covalent derivatization and separation of their diastereomeric amides with (R)- or (S)-α- arylethylamines.

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