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ChemicalBook >  Product Catalog >  Chemical Reagents >  Organic reagents >  Thiolate >  3,4,5,6-TETRAHYDRO-2-PYRIMIDINETHIOL

3,4,5,6-TETRAHYDRO-2-PYRIMIDINETHIOL

Basic information Uses Safety Supplier Related

3,4,5,6-TETRAHYDRO-2-PYRIMIDINETHIOL Basic information

Product Name:
3,4,5,6-TETRAHYDRO-2-PYRIMIDINETHIOL
Synonyms:
  • n,n’-trimethylenethiourea
  • N,N'-Trimethylenethiourea
  • Perhydropyrimidine-2-thione
  • tetrahydro-2(1h)-pyrimidinethion
  • Tetrahydro-2(1H)-pyrimidinethione
  • Tetrahydropyrimidine-2-thione
  • Thiourea, N,N'-1,3-propanediyl-
  • 3,4,5,6-tetrahydropyrimidine-2-thiol
CAS:
2055-46-1
MF:
C4H8N2S
MW:
116.18
EINECS:
218-152-3
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • Pyrimidines
Mol File:
2055-46-1.mol
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3,4,5,6-TETRAHYDRO-2-PYRIMIDINETHIOL Chemical Properties

Melting point:
210-212 °C (lit.)
Boiling point:
171.6±23.0 °C(Predicted)
Density 
1.095 (estimate)
refractive index 
1.5000 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO (Slightly), Methanol (Slightly)
pka
14.98±0.20(Predicted)
form 
solid
color 
White to Off-White
CAS DataBase Reference
2055-46-1(CAS DataBase Reference)
EPA Substance Registry System
Propylenethiourea (2055-46-1)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
RTECS 
UW5782000
HazardClass 
IRRITANT
HS Code 
29335990

MSDS

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3,4,5,6-TETRAHYDRO-2-PYRIMIDINETHIOL Usage And Synthesis

Uses

Tetrahydropyrimidine-2(1H)-thione is a reactant in the preparation of aryl substituted heterocycles.

Uses

Tetrahydropyrimidine-2(1H)-thione is a reactant in the preparation of aryl substituted heterocycles.

Preparation

The preparation of 3,4,5,6-Tetrahydro-2- pyrimidinethiol is as follows:Carbon disulfide (0.2 mol) was added dropwise to a  solution of 1,3-diamino propane 1 (0.2 mol) in H2O/EtOH  (20 ml), and the temperature was remained constant at  0-5 oC. After the completion of addition, the reaction  mixture was refluxed for 12h and then cooled to room  temperature. The precipitate was collected by filtration and  recrystallized from EtOH to give pure desired compound.

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