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1-amino-3-(4-methylphenoxy)propan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55776-85-7

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55776-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55776-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,7 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55776-85:
(7*5)+(6*5)+(5*7)+(4*7)+(3*6)+(2*8)+(1*5)=167
167 % 10 = 7
So 55776-85-7 is a valid CAS Registry Number.

55776-85-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-amino-3-(4-methylphenoxy)propan-2-ol

1.2 Other means of identification

Product number -
Other names HMS1692D14

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:55776-85-7 SDS

55776-85-7Relevant academic research and scientific papers

Tricyclic compound derivatives useful in the treatment of neoplastic diseases, inflammatory disorders and immunomodulatory disorders

-

Page/Page column 58, (2008/12/06)

Provided are compounds of the formula (I): or a stereoisomer, tautomer, salt, hydrate or prodrug thereof that modulate tyrosine kinase activity, compositions comprising the compounds and methods of their use.

Reactions of 1,2- and 1,3-amino-alcohols with imidate salts and with ortho esters

Butt, Mohammed I.,Neilson, Douglas G.,Watson, Kathleen M.,Zakir-Ullah

, p. 2328 - 2332 (2007/10/04)

ω-Hydroxy-N-substituted amidines have been shown to be the intermediates in the formation of 2-oxazolines and 5,6-dihydro-4H-1,3-oxazines from the reactions of imidates and 1,2- and 1,3-amino-alcohols respectively, 1,2- and 1,3-Amino-alcohols also react with ortho esters to give 2-oxazolines and 5,6-dihydro-4H-1,3-oxazines, but N-acylamino-alcohols give rise to oxazolidines with ortho esters.

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