50698-76-5 Usage
Uses
Used in Pharmaceutical Applications:
S-(carboxymethyl)-D-cysteine is used as a therapeutic agent for the treatment of acetaminophen overdose, where it helps in reducing liver damage caused by the toxic effects of the drug.
Used in Respiratory Disease Management:
In the healthcare industry, S-(carboxymethyl)-D-cysteine is used as a management tool for chronic obstructive pulmonary disease (COPD) and cystic fibrosis, where its antioxidant properties contribute to alleviating symptoms and improving lung function.
Used in Psychiatric Disorder Treatment:
S-(carboxymethyl)-D-cysteine is being studied for its potential use as a treatment for psychiatric disorders, leveraging its antioxidant and detoxification properties to support mental health.
Used in Respiratory Infection Treatment:
In the medical field, S-(carboxymethyl)-D-cysteine is being explored for its potential in treating respiratory infections, where its immune-modulating and antioxidant effects may contribute to improved respiratory health.
Used in Liver Function Improvement and Detoxification:
S-(carboxymethyl)-D-cysteine is being researched for its potential to enhance liver function and support detoxification processes, which can be beneficial in various liver-related health conditions.
Used in Dietary Supplements:
As a dietary supplement, S-(carboxymethyl)-D-cysteine is used to provide additional antioxidant support, which can contribute to overall health and well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 50698-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,9 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50698-76:
(7*5)+(6*0)+(5*6)+(4*9)+(3*8)+(2*7)+(1*6)=145
145 % 10 = 5
So 50698-76-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO4S/c7-4(8)1-6-3(2-11)5(9)10/h3,6,11H,1-2H2,(H,7,8)(H,9,10)/t3-/m1/s1
50698-76-5Relevant academic research and scientific papers
Optical Resolution of Racemic S-(Carboxymethyl)cysteine
Kleemann, Axel,Martens, Juergen
, p. 1995 - 1998 (2007/10/02)
Racemic S-(carboxymethyl)cysteine obtained from racemic cysteine is resolved via its ammonium salt (R,S)-3 by preferential crystallization procedure.Furthermore, (R,S)-2 forms with optically active amines separable, diastereomeric salts.Thus, (1R,2S)-2-amino-1-phenyl-1-propanol (4) affords optically pure (R)-S-(carboxymethyl)cysteine in 93 percent yield.The resolution of (R,S)-2 is also possible with (R)-1-phenylethylamine (5).
