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(S)-2-Isopropyl-2,3-dihydrobenzo[d]imidazo[2,1-b]thiazole

  • CAS No. 1214921-55-7

  • Cat. No. CS-0145083
  • Purity≥98%
  • MDL No.MFCD33395897

*For research and further manufacturing use only, not for direct human use.

(S)-2-Isopropyl-2,3-dihydrobenzo[d]imidazo[2,1-b]thiazole|CS-0145083

Structure of 1214921-55-7

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General Information

  • CAS No. 1214921-55-7
  • Cat. No. CS-0145083
  • Purity ≥98%
  • MDL No. MFCD33395897
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₂H₁₄N₂S
  • Molecular Weight 218.32
  • Synonym(s) None
  • SMILES CC(C)[C@H]1CN2C3=CC=CC=C3SC2=N1

Description

(S)-2-Isopropyl-2,3-dihydrobenzo[d]imidazo[2,1-b]thiazole is a chiral heterocyclic scaffold featuring a fused imidazothiazole core with defined stereochemistry at the 2-position. This configuration imparts distinct conformational rigidity and directional polarity, enabling precise molecular recognition in asymmetric synthesis. The isopropyl substituent enhances solubility and steric profile, improving compatibility in catalytic systems and medicinal chemistry applications.

Application

(S)-2-Isopropyl-2,3-dihydrobenzo[d]imidazo[2,1-b]thiazole serves as a synthetically valuable chiral heterocyclic scaffold, enabling access to biologically relevant imidazothiazole frameworks. Its bench-stable structure features orthogonal functionalization sites, facilitating downstream derivatization via electrophilic substitution or transition-metal-catalyzed coupling. The stereogenic center supports enantioselective synthesis applications in medicinal chemistry and catalyst design.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P280-P302+P352

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Computational Chemistry Data

  • TPSA   15.6
  • LogP   2.9929
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   1

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