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benzyl (2R)-2-benzyl-3<<<2-<(methoxyethoxy)methoxy>ethyl>methylamino>carbonyl>propionate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122225-47-2

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122225-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122225-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,2,2 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 122225-47:
(8*1)+(7*2)+(6*2)+(5*2)+(4*2)+(3*5)+(2*4)+(1*7)=82
82 % 10 = 2
So 122225-47-2 is a valid CAS Registry Number.

122225-47-2SDS

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 benzyl (2R)-2-benzyl-3[[[2-[(methoxyethoxy)methoxy]ethyl]methylamino]carbonyl]propionate

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:122225-47-2 SDS

122225-47-2Relevant academic research and scientific papers

Water-Soluble Renin Inhibitors: Design of a Subnanomolar Inhibitor with a Prolonged Duration of Action

Rosenberg, Saul H.,Woods, Keith W.,Sham, Hing L.,Kleinert, Hollis D.,Martin, Donald L.,et al.

, p. 1962 - 1969 (2007/10/02)

Incorporation of nonreactive polar functionalities at the C- and N-termini of renin inhibitors led to the development of a subnanomolar compound (21) with millimolar solubility.This inhibitor demonstrated excellent efficacy and a long duration of action upon intravenous administration to monkeys.While activity was also observed intraduodenally, a comparison of the blood pressure responses indicated low bioavailability.Subsequent experiments in rats showed that, although the compound was absorbed from the gastrointrestinal tract, extensive liver extraction severely limited bioavailability.

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