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109417-60-9

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109417-60-9 Usage

Physical state

Colorless to pale yellow liquid

Odor

Strong

Usage

Production of pharmaceuticals, fragrances, intermediate in organic synthesis, production of herbicides and insecticides

Potential medical application

Treatment of cardiovascular and endocrine disorders

Precaution

Handle with caution due to potential health hazards and environmental impact

Check Digit Verification of cas no

The CAS Registry Mumber 109417-60-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,4,1 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 109417-60:
(8*1)+(7*0)+(6*9)+(5*4)+(4*1)+(3*7)+(2*6)+(1*0)=119
119 % 10 = 9
So 109417-60-9 is a valid CAS Registry Number.

109417-60-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-2-(2-methoxyethoxy)benzene

1.2 Other means of identification

Product number -
Other names (2-methoxyethoxy)bromobenzene

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:109417-60-9 SDS

109417-60-9Relevant articles and documents

FUSED RING PYRIMIDINE COMPOUND, INTERMEDIATE, AND PREPARATION METHOD, COMPOSITION AND USE THEREOF

-

Paragraph 0157-0158, (2018/08/12)

Disclosed area fused ring pyrimidine compound, and an intermediate, a preparation method, a composition and a use thereof. The fused ring pyrimidine compound is a compound as shown in formula I, a tautomer, an enantiomer, a diastereoisomer, a pharmaceutically acceptable salt, a metabolite, a metabolic precursor or a prodrug thereof, wherein the above-mentioned compound is used for the preparation of a medicine for preventing, remitting or treating one or more of immune system diseases, autoimmune diseases, cell proliferative diseases, allergic disorders and cardiovascular diseases, and the compound has a strong inhibitory effect on the Janues kinase, FGFR kinase, FLT3 kinase and Src family kinase.

Identification of a new biaryl scaffold generating potent renin inhibitors

Lacombe, Patrick,Aspiotis, Renée,Bayly, Christopher,Chen, Austin,Dubé, Daniel,Fortin, Réjean,Gallant, Michel,Juteau, Hélne,Liu, Suzanna,McKay, Dan,Roy, Patrick,Wu, Tom

scheme or table, p. 5822 - 5826 (2010/12/19)

The discovery and SAR of a series of potent renin inhibitors possessing a novel biaryl scaffold are described herein. Molecular modeling revealed that the cyclopropylamide spacer present in 1 can be replaced by a simple, substituted aromatic ring such as

Chiral Induction in the Methylation of N-Ethoxycarbonylmethyl Sulfoximines

Hambley, Trevor W.,Raguse, Burkhard,Ridley, Damon D.

, p. 1833 - 1842 (2007/10/02)

Chiral inductions in the C-methylations of four optically active N-ethoxycarbonylmethyl-S-p-tolylsulfoximines were explored by using the reagents lithium diisopropylamide (in tetrahydrofuran at -78 deg) then methyl iodide.When the fourth substituent at su

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