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1015070-59-3

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  • Benzenepropanoic acid, -[2-[[(1,1-dimethylethoxy)carbonyl]amino]ethyl]-

    Cas No: 1015070-59-3

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1015070-59-3 Usage

General Description

Benzenepropanoic acid, -[2-[[(1,1-dimethylethoxy)carbonyl]amino]ethyl]-, also known as Ibuprofen lysine, is a nonsteroidal anti-inflammatory drug (NSAID) that is used to relieve pain, reduce inflammation, and lower fevers. It works by inhibiting the production of prostaglandins, which are chemicals that play a role in causing pain and inflammation in the body. Ibuprofen lysine is commonly used to treat conditions such as arthritis, menstrual cramps, and muscle aches. It is available in various forms, including tablets, capsules, and oral suspensions, and is generally well-tolerated when used as directed, although it can cause side effects such as stomach irritation and increased risk of heart attack or stroke.

Check Digit Verification of cas no

The CAS Registry Mumber 1015070-59-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,5,0,7 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1015070-59:
(9*1)+(8*0)+(7*1)+(6*5)+(5*0)+(4*7)+(3*0)+(2*5)+(1*9)=93
93 % 10 = 3
So 1015070-59-3 is a valid CAS Registry Number.

1015070-59-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-4-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid

1.2 Other means of identification

Product number -
Other names 4-[(tert-butoxy)carbonylamino]-2-benzylbutanoic acid

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:1015070-59-3 SDS

1015070-59-3Upstream product

1015070-59-3Downstream Products

1015070-59-3Relevant articles and documents

Substituted Hantzsch Esters as Versatile Radical Reservoirs in Photoredox Reactions

Gu, Fangjun,Huang, Wenhao,Liu, Xu,Chen, Wenxin,Cheng, Xu

supporting information, p. 925 - 931 (2018/01/04)

Substituted Hantzsch esters can act as radical reservoirs in photoredox reactions, steadily releasing a carbon radical and a hydrogen atom radical in the absence of an additional electron acceptor. We propose that radical release by substituted Hantzsch esters occurs via a mechanism involving an internal redox cycle. Cinnamidecinnamides, styrenes, α,β-unsaturated acids, and diarylethenes could be alkylated smoothly with these reagents. (Figure presented.).

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