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1173022-25-7

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1173022-25-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1173022-25-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,0,2 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1173022-25:
(9*1)+(8*1)+(7*7)+(6*3)+(5*0)+(4*2)+(3*2)+(2*2)+(1*5)=107
107 % 10 = 7
So 1173022-25-7 is a valid CAS Registry Number.

1173022-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-acetyloxybenzoic acid

1.2 Other means of identification

Product number -
Other names Acetylsalicylic acid-|A-13C

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:1173022-25-7 SDS

1173022-25-7Relevant articles and documents

Real-Time Interrogation of Aspirin Reactivity, Biochemistry, and Biodistribution by Hyperpolarized Magnetic Resonance Spectroscopy

Zacharias, Niki M.,Ornelas, Argentina,Lee, Jaehyuk,Hu, Jingzhe,Davis, Jennifer S.,Uddin, Nasir,Pudakalakatti, Shivanand,Menter, David G.,Karam, Jose A.,Wood, Christopher G.,Hawk, Ernest T.,Kopetz, Scott,Vilar, Eduardo,Bhattacharya, Pratip K.,Millward, Steven W.

supporting information, p. 4179 - 4183 (2019/02/25)

Hyperpolarized magnetic resonance spectroscopy enables quantitative, non-radioactive, real-time measurement of imaging probe biodistribution and metabolism in vivo. Here, we investigate and report on the development and characterization of hyperpolarized acetylsalicylic acid (aspirin) and its use as a nuclear magnetic resonance (NMR) probe. Aspirin derivatives were synthesized with single- and double-13C labels and hyperpolarized by dynamic nuclear polarization with 4.7 % and 3 % polarization, respectively. The longitudinal relaxation constants (T1) for the labeled acetyl and carboxyl carbonyls were approximately 30 seconds, supporting in vivo imaging and spectroscopy applications. In vitro hydrolysis, transacetylation, and albumin binding of hyperpolarized aspirin were readily monitored in real time by 13C-NMR spectroscopy. Hyperpolarized, double-labeled aspirin was well tolerated in mice and could be observed by both 13C-MR imaging and 13C-NMR spectroscopy in vivo.

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