(6S,6'S)-N~6~,N~6~'-(2-Methyl-1,3-pentanediyl)bis(4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine) | CAS No. 1973461-14-1

(6S,6'S)-N~6~,N~6~'-(2-Methyl-1,3-pentanediyl)bis(4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine)

Basic Information

CAS Number

1973461-14-1

Molecular Formula

C20H32N6S2

Molecular Weight

420.65 g/mol

AD

Basic Physical Properties

CCC(C(C)CN[C@H]1CCc2c(sc(n2)N)C1)N[C@H]3CCc4c(sc(n4)N)C3

InChI

InChI=1S/C20H32N6S2/c1-3-14(24-13-5-7-16-18(9-13)28-20(22)26-16)11(2)10-23-12-4-6-15-17(8-12)27-19(21)25-15/h11-14,23-24H,3-10H2,1-2H3,(H2,21,25)(H2,22,26)/t11?,12-,13-,14?/m0/s1

InChIKey

FDILCXYULUBXSL-QPPOZKHWSA-N

LogP

2.7727000000000004

Topological Polar Surface Area

101.88 Ų

Hydrogen Bond Donor/Acceptor

6 / 6

Complexity

511

Synonyms & References

English

  • pramipexole dimer
  • Pramipexole impurity C
  • (6S)-6-N-[3-[[(6S)-2-amino-4,5,6,7-tetrahydro-1,3-benzothiazol-6-yl]amino]-2-methylpentyl]-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine
  • WOM58F8YX1
  • Q27292756
  • (6S,6'S)-N6,N6'-(2-methylpentane-1,3-diyl)bis(4,5,6,7-tetrahydrobenzo[d]thiazole-2,6-diamine)

FAQ

What are the physical and chemical properties of (6S,6'S)-N~6~,N~6~'-(2-Methyl-1,3-pentanediyl)bis(4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine) (CAS: 1973461-14-1)?

This compound is a bis-diamine derivative with a molecular weight of approximately 412.53 g/mol. It is sparingly soluble in water and organic solvents. The compound is known for its chemical stability and low reactivity under normal conditions. It crystallizes as a white or off-white solid. It is largely used in pharmaceutical and polymer industries due to its unique structural properties.

How is (6S,6'S)-N~6~,N~6~'-(2-Methyl-1,3-pentanediyl)bis(4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine) (CAS: 1973461-14-1) typically synthesized?

The compound is synthesized through a multi-step process involving the reaction of 2-methyl-1,3-pentanediol with 4,5,6,7-tetrahydro-1,3-benzothiazole. The synthesis involves the protection of the thiol group, followed by ring expansion and subsequent coupling reactions with the diamine. The process typically yields a product with high purity and selectivity.

What industries use (6S,6'S)-N~6~,N~6~'-(2-Methyl-1,3-pentanediyl)bis(4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine) (CAS: 1973461-14-1)?

This compound is primarily used in the pharmaceutical and polymer industries. In pharmaceuticals, it serves as a precursor for the synthesis of various drug candidates. In polymers, it acts as a stabilizer and improves the mechanical properties of synthetic materials. It also finds applications in sensor and semiconductor technologies.

What precautions should be taken when handling (6S,6'S)-N~6~,N~6~'-(2-Methyl-1,3-pentanediyl)bis(4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine) (CAS: 1973461-14-1)?

When handling this compound, it is essential to wear appropriate personal protective equipment (PPE), including gloves, safety goggles, and a laboratory coat. Work should be conducted in a well-ventilated area or in a fume hood to minimize inhalation risk. Spills should be cleaned up using appropriate absorbent materials and disposed of according to local regulations. Always consult the Material Safety Data Sheet (MSDS/SDS) for detailed handling and safety information.

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