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4-(HYDROXYMETHYL)PHENYLACETIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73401-74-8

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73401-74-8 Usage

Chemical Properties

White solid

Check Digit Verification of cas no

The CAS Registry Mumber 73401-74-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,0 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 73401-74:
(7*7)+(6*3)+(5*4)+(4*0)+(3*1)+(2*7)+(1*4)=108
108 % 10 = 8
So 73401-74-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O3/c10-6-8-3-1-7(2-4-8)5-9(11)12/h1-4,10H,5-6H2,(H,11,12)

73401-74-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H27531)  4-(Hydroxymethyl)phenylacetic acid, 98%   

  • 73401-74-8

  • 1g

  • 311.0CNY

  • Detail
  • Alfa Aesar

  • (H27531)  4-(Hydroxymethyl)phenylacetic acid, 98%   

  • 73401-74-8

  • 5g

  • 1178.0CNY

  • Detail

73401-74-8SDS

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 2-(4-(Hydroxymethyl)phenyl)acetic acid

1.2 Other means of identification

Product number -
Other names 2-[4-(hydroxymethyl)phenyl]acetic acid

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:73401-74-8 SDS

73401-74-8Relevant articles and documents

Preparation method of netarsudil mesylate

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, (2021/07/17)

The invention relates to a preparation method of netarsudil mesylate.Netarsudil mesylate is synthesized by utilizing chiral induction, and compared with an existing chiral HPLC method or SFC method, netarsudil mesylate prepared by adopting a chemical synt

Nitroxide derivative of ROCK kinase inhibitor

-

, (2020/06/17)

The invention provides a small molecular compound of a NO donor. The small molecular compound is characterized in that the small molecular compound is a compound shown represented by structural formula I shown in the description, or a stereoisomer, a geometrical isomer, a tautomer, a racemate, a deuterated isotope derivative, a hydrate, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrug thereof; and in the formula I, ring A is a substituted or unsubstituted heteroaromatic ring, X is selected from (CH2)n, n is selected from 0, 1, 2 and 3, R is a substituent group of terminal -O-NO2, R is selected from hydrogen, a hydroxyl group, halogen, an amino group, a cyano group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted alkynyl group and a substituted or unsubstituted heteroalkyl group, and R and R are respectively and independently selected from hydrogen, a substituted or unsubstituted alkyl group, a substituted or unsubstituted naphthenic base or an amino protecting group, or R and R are connected to form a substituted or unsubstituted cyclic heteroalkyl group. The compound has a high-activity inhibition effect on ROCK kinase.

Process for the preparation of kinase inhibitors and intermediates thereof

-

, (2017/05/31)

Described are processes for the synthesis of certain compounds, useful for treating diseases, e.g. eye disease, such as glaucoma and ocular hypertension, in a subject.

PROCESS FOR THE PREPARATION OF KINASE INHIBITORS AND INTERMEDIATES THEREOF

-

, (2017/06/12)

Described are processes for the synthesis of certain compounds, useful for treating diseases, e.g. eye disease, such as glaucoma and ocular hypertension, in a subject.

Preparation method of AR-13324

-

, (2018/03/28)

The invention relates to a preparation method of AR-13324. According to the invention, a chiral ligand is used for chiral induced synthesis of AR-13324. In comparison with an existing chiral HPLC method or a SFC method, the method of the invention has the

Substituted aromatic amides and ureas derivatives having anti-hypercholesteremic activity, their preparation and their therapeutic uses

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, (2008/06/13)

Compounds of formula (I) are provided: STR1 wherein: R1 represents an alkyl group; or a group of formula (II), (III), (IV) or (V): STR2 and wherein the groups R2, R3, R4 and R5 are hydrogen or various organic groups; and pharmaceutically acceptable salts thereof; as well as methods for the preparation of such compounds and their use in the treatment and prophylaxis of hypercholesteremia and arteriosclerosis.

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