22572-33-4 Usage
Description
2-(Benzylthio)ethyamine hydrochloride, also known as S-Benzylcysteamine hydrochloride, is a sulfur-containing organic building block derived from the reaction of S-benzylcysteamine with 0.1M methanolic NaOMe. It is a versatile compound with potential applications in various industries due to its unique chemical properties.
Uses
Used in Pharmaceutical Industry:
2-(Benzylthio)ethyamine hydrochloride is used as a starting reagent for the synthesis of mercaptoacetyltriglycine (MAG3) derivatives. These derivatives are essential in the development of radiopharmaceuticals, particularly for diagnostic imaging applications in nuclear medicine. The compound's ability to form MAG3 derivatives makes it a valuable component in the creation of imaging agents that can help detect and monitor various medical conditions.
Used in Chemical Synthesis:
As a sulfur-containing organic building block, 2-(Benzylthio)ethyamine hydrochloride can be utilized in the synthesis of various organic compounds and pharmaceuticals. Its unique structure allows for the formation of new chemical entities with potential applications in different industries, including pharmaceuticals, agrochemicals, and materials science. The compound's versatility in chemical reactions makes it a valuable asset in the development of novel products and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 22572-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,7 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22572-33:
(7*2)+(6*2)+(5*5)+(4*7)+(3*2)+(2*3)+(1*3)=94
94 % 10 = 4
So 22572-33-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NS/c10-6-7-11-8-9-4-2-1-3-5-9/h1-5H,6-8,10H2/p+1
22572-33-4Relevant articles and documents
Synthesis and biological characteristics of the technetium-99m triamide derivatives of mercaptoacetyltriglycine (MAG3)
Okarvi,Adriaens,Verbruggen
, p. 73 - 84 (2007/10/03)
A number of MAG3-derivatives, containing the three-amide functions modified by inverting the sequence -CO-NH- to -NH-CO- in the first-and/or second-amide functions, have been labelled with 99mTc in order to study the renal characteristics of the resulting MAG3-derivatives versus the reference 99mTc-MAG3. The 99mTc-MAG3-derivatives displayed HPLC-profiles similar to that of 99mTc-MAG3. Furthermore, in mice they exhibited biological behaviour comparable or even superior to 99mTc-MAG3, which indicates that the sequence of the first- and/or second-amide bond in 99mTc-MAG3 affects the biological behaviour only to a limited degree. However, in baboon the plasma clearance of the 99mTc-MAG3-derivatives was relatively slower than 99mTc-MAG3, which underlines the inter-species variability. Copyright
Studies Relating to the Ferredoxins. Part 3. The Synthesis of Some Cysteine-Glycine Peptides for Iron-Sulphur Complexing Studies
Balasubramaniam, Ambikaipakan,Burt, Roger J.,Christou, George,Ridge, Brian,Rydon, H. N.
, p. 310 - 317 (2007/10/02)
Three peptides with the general structure Ac-Gly2.(Cys.Glym)n.Cys.Gly3.Cys.Gly2.NH2 (1; m = 2 or 3; n = 0 or 1), four with the general structure Ac.Gly2.Cysn.Gly2.NH2
