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(3S,4S)-4-AMINO-1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-OL is a chemical compound belonging to the class of organic compounds known as penicillins. It is a beta-lactam antibiotic with a molecular formula of C4H5NO3S. (3S,4S)-4-AMINO-1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-OL features a tetrahydrothiophene ring with an amino group and a dioxo group attached to it, which contributes to its effectiveness as an antibiotic.

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  • 20688-37-3 Structure
  • Basic information

    1. Product Name: (3S,4S)-4-AMINO-1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-OL
    2. Synonyms: (3S,4S)-4-AMINO-1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-OL;(3S,4S)-4-AMINOTETRAHYDROTHIOPHENE-3-OL 1,1-DIOXIDE;4-Aminotetrahydro-3-thiophenol 1,1-dioxide;Aids127391;Aids-127391;Nsc160588;(3S,4S)-4-aminotetrahydrothiophene-3-ol 1,1-dioxide(SALTDATA: FREE);4-amino-1,1-diketo-thiolan-3-ol
    3. CAS NO:20688-37-3
    4. Molecular Formula: C4H9NO3S
    5. Molecular Weight: 151.18416
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 20688-37-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 424.1°Cat760mmHg
    3. Flash Point: 210.3°C
    4. Appearance: /
    5. Density: 1.514g/cm3
    6. Vapor Pressure: 5.73E-09mmHg at 25°C
    7. Refractive Index: 1.563
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (3S,4S)-4-AMINO-1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-OL(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3S,4S)-4-AMINO-1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-OL(20688-37-3)
    12. EPA Substance Registry System: (3S,4S)-4-AMINO-1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-OL(20688-37-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 20688-37-3(Hazardous Substances Data)

20688-37-3 Usage

Uses

Used in Pharmaceutical Industry:
(3S,4S)-4-AMINO-1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-OL is used as an antibiotic medication for treating a variety of bacterial infections. Its chemical structure and properties make it effective against infections such as respiratory, skin, and urinary tract infections. As a member of the penicillin class, it plays a crucial role in the medical field for combating bacterial diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 20688-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,8 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20688-37:
(7*2)+(6*0)+(5*6)+(4*8)+(3*8)+(2*3)+(1*7)=113
113 % 10 = 3
So 20688-37-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H9NO3S/c5-3-1-9(7,8)2-4(3)6/h3-4,6H,1-2,5H2/t3-,4-/m1/s1

20688-37-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4S)-4-AMINO-1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-OL

1.2 Other means of identification

Product number -
Other names 3-hydroxy-4-aminothiolane 1,1-dioxide

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:20688-37-3 SDS

20688-37-3Relevant articles and documents

Structure-activity studies of cyclic ketone inhibitors of the serine protease plasmin: Design, synthesis, and biological activity

Xue, Fengtian,Seto, Christopher T.

, p. 8467 - 8487 (2008/02/05)

Three series of cyclic ketone inhibitors were synthesized and evaluated against the serine protease plasmin. Peptide inhibitors that incorporated 3-oxotetrahydrofuran and 3-oxotetrahydrothiophene 1,1-dioxide groups had the highest activities. Alkylamino substituents, which were designed to bind in the S1 subsite of plasmin, were attached to the inhibitors. Compounds 5c and 5g, which incorporated 6-aminohexyl substituents, were found to be optimal and demonstrated IC50 values in the low micromolar range. Incorporating conformationally constrained peptide segments into the inhibitors did not improve their activities.

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