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103889-84-5

103889-84-5

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103889-84-5 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 103889-84-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,8,8 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 103889-84:
(8*1)+(7*0)+(6*3)+(5*8)+(4*8)+(3*9)+(2*8)+(1*4)=145
145 % 10 = 5
So 103889-84-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO3/c1-13-7-5-3-2-4-6(7)8(10)9(11)12/h2-5,8H,10H2,1H3,(H,11,12)

103889-84-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-2-METHOXY-PHENYLGLYCINE

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:103889-84-5 SDS

103889-84-5Relevant articles and documents

ISOINDOLIN-1-ON DERIVATIVE, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION COMPRISING SAME AS EFFECTIVE COMPONENT FOR PREVENTING OR TREATING CANCER

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Paragraph 0092; 0094, (2021/06/25)

The present invention relates to an isoindolin-1-one derivative, a method for preparing the same, and a pharmaceutical composition comprising the same as an active ingredient for preventing or treating cancer, wherein the isoindolin-1-one derivative exhib

A practical asymmetric synthesis of homochiral α-arylglycines

Mellin-Morliere, Christelle,Aitken, David J.,Bull, Steven D.,Davies, Stephen G.,Husson, Henri-Philippe

, p. 149 - 155 (2007/10/03)

Enantioselective reduction of a series of substituted aryl trichloromethyl ketones with the CBS-catecholborane reagent afforded homochiral aryl trichloromethyl carbinols which have been elaborated to give homochiral α-arylglycines in high e.e.

SYNTHESIS OF 2,3-BENZO-1-OXAOCTEM-4-CARBOXYLIC ACID

Daum, S. J.,Hansen, P. E.

, p. 1 - 6 (2007/10/02)

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