Scabioside C | CAS No. 17233-22-6

Scabioside C

Basic Information

CAS Number

17233-22-6

Molecular Formula

C41H66O13

Molecular Weight

766.95 g/mol

AD

Basic Physical Properties

Physical State

Powder

Melting Point

242-244 ºC

Solubility

Insuluble (5.7E-4 g/L) (25 ºC),

OCC1OC(OC2COC(C(C2O)O)OC2CCC3(C(C2(C)CO)CCC2(C3CC=C3C2(C)CCC2(C3CC(C)(C)CC2)C(=O)O)C)C)C(C(C1O)O)O

InChI

InChI=1S/C41H66O13/c1-36(2)13-15-41(35(49)50)16-14-39(5)21(22(41)17-36)7-8-26-37(3)11-10-27(38(4,20-43)25(37)9-12-40(26,39)6)54-33-31(47)29(45)24(19-51-33)53-34-32(48)30(46)28(44)23(18-42)52-34/h7,22-34,42-48H,8-20H2,1-6H3,(H,49,50)

InChIKey

KAYMPWXMHIUNGC-UHFFFAOYSA-N

LogP

2.493500000000003

Topological Polar Surface Area

215.82999999999998 Ų

Hydrogen Bond Donor/Acceptor

8 / 13

Complexity

1460

Synonyms & References

English

  • Scabioside C
  • (3β)-3-{[4-O-(β-D-Glucopyranosyl)-α-L-arabinopyranosyl]oxy}-23-hy droxyolean-12-en-28-oic acid
  • [3H]-Brotizolam
  • 2-Brom-4-(2-chlorphenyl)-9-methyl-6H-thieno<3,2-f><1,2,4>triazolo<4,3-a>1,4>diazepin
  • 2-bromo-4-(2-chlorophenyl)-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine
  • acirc
  • Brotizolamum [INN-Latin]
  • -D-glucopyranosyl-R-Larabinopyranosyl) oxy]-23-hydroxy-,(3&acirc
  • Lendorm
  • Lendormin
  • Lendormin(R)
  • Leontosid B
  • leontoside B
  • WE-941
  • 8256AH

MDL Number

MFCD28124359

FAQ

What are the physical and chemical properties of Scabioside C (CAS: 17233-22-6)?

Scabioside C is a naturally occurring flavonol glycoside. It is a white or off-white crystalline powder with a molecular weight of approximately 482.3 g/mol. It is slightly soluble in water and ethanol but poorly soluble in organic solvents. Chemically, it is relatively stable under normal conditions but can react with acids to release aglycone. It is commonly used in pharmaceutical and cosmetic industries due to its antioxidant and anti-inflammatory properties.

How is Scabioside C (CAS: 17233-22-6) typically synthesized?

Scabioside C is typically synthesized through the glycosylation of flavonols using acetic acid and a suitable glycosyl donor. Common catalysts include sodium hydride and HATU (O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate). The yield is usually around 70-80% under optimal conditions. The reaction involves careful control of pH and temperature to ensure selectivity and yield.

What industries use Scabioside C (CAS: 17233-22-6)?

Scabioside C is used in the pharmaceutical industry for its antioxidant and anti-inflammatory properties. It is also utilized in the cosmetic industry for its skin-protecting and anti-aging effects. Additionally, it has potential applications in the food industry as a natural colorant and antioxidant. Its use in polymer production for enhanced properties and in sensors for detecting specific compounds is also being explored.

What precautions should be taken when handling Scabioside C (CAS: 17233-22-6)?

When handling Scabioside C, it is advisable to wear gloves, goggles, and a lab coat to protect against skin and eye contact. It should be stored in a cool, dry place away from direct sunlight and moisture to prevent degradation. In case of a spill, use appropriate personal protective equipment (PPE) and clean up immediately using a suitable absorbent material. Always refer to the Safety Data Sheet (SDS) for detailed handling and emergency procedures.

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