77489-36-2

Basic information

• Product Name: Hepta-O-acetyl-β-D-lactosyl-isothiocyanate
• Synonyms: Hepta-O-acetyl-β-D-lactosyl-isothiocyanate;2,3,6,2',3',4',6'-Hepta-O-acetyl-b-D-lactosyl isothiocyanate;4-O-(2,3,4,6-Tetra-O-acetyl-beta-D-galactopyranosyl)-beta-D-glucopyranosyl isothiocyanate 2,3,6-triacetate;Hepta-O-acetyl-beta-D-lactosyl isothiocyanate
• CAS NO: 77489-36-2
• Molecular Formula: C₂₇H₃₅NO₁₇S
• Molecular Weight: 677.63
• Product Categories: Carbohydrates
• Mol File: 77489-36-2.mol
• Article Data: 19

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Hepta-O-acetyl-β-D-lactosyl-isothiocyanate(CAS DataBase Reference)
• NIST Chemistry Reference: Hepta-O-acetyl-β-D-lactosyl-isothiocyanate(77489-36-2)
• EPA Substance Registry System: Hepta-O-acetyl-β-D-lactosyl-isothiocyanate(77489-36-2)

Safety Data

• Hazardous Substances Data: 77489-36-2(Hazardous Substances Data)

Upstream product

• 333-20-0 potassium thioacyanate 
• 5160-10-1 2,3,6-tetra-O-acetyl-4-O-(2',3',4',6'-tetra-O-acetyl-β-D-galactopyranosyl)-D-glucopyranosylbromide 
• 70223-97-1 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-acetyl-β-D-glucopyranosyl bromide 
• 943860-89-7 C₂₆H₃₅NO₁₆ 
• 463-71-8 thiophosgene 
• 3616-19-1 lactose octaacetate 
• 592-87-0 lead(II) thiocyanate 
• 4753-07-5 2,3,6,2',3',4',6'-hepta-O-acetyl-lactosyl bromide 
• 63-42-3 D-(+)-lactose 
• 1147550-11-5 ammonium thiocyanate 
• 4753-07-5 α-hepta-O-acetylmaltosyl bromide 
• 943860-88-6 C₂₆H₃₅NO₁₆ 
• 4753-07-5 2,3,6,2',3',4',6'-hepta-O-acetyl-α-D-maltosyl bromide 
• 69-79-4 D-maltose 

Downstream Products

• 1311163-37-7 C₃₄H₄₂N₄O₁₉S 
• 1311163-38-8 C₃₄H₄₂N₄O₁₉S 
• 1311163-39-9 C₃₄H₄₂ClN₃O₁₇S 
• 1311163-40-2 C₃₄H₄₁Cl₂N₃O₁₇S 
• 1311163-41-3 C₃₄H₄₂BrN₃O₁₇S 
• 1311163-42-4 benzaldehyde 2,3,6,2',3',4',6'-hepta-O-acetyl-β-maltosyl thiosemicarbazone 
• 1311163-43-5 C₃₇H₄₉N₃O₁₇S 
• 1311163-44-6 C₃₅H₄₅N₃O₁₈S 
• 1311163-45-7 C₃₆H₄₇N₃O₁₉S 
• 1311163-46-8 C₃₄H₄₃N₃O₁₈S 
• 1311163-47-9 C₃₄H₄₃N₃O₁₈S 

Relevant articles and documents

Synthesis and characterization of some novel thiosemicarbazones of substituted benzaldehydes and N-(Hepta-O-Acetyl-β-D-Lactosyl) thiosemicarbazide

A set of reaction conditions, including ionic liquids as catalysts, water as solvent and microwave-assisted heating method, had been investigated for the synthesis of hepta-O-acetyl-β-D-lactosyl thiosemicarbazones. Based on optimized conditions, namely, [

Synthesis and Antimicrobial Activities of 1,2,4-Thiadiazolidin-3-thione Hydrochlorides

Synthesis of N-glucosyl/lactosyl/maltosyl-1,2,4-thiadizolidin-3-thione hydrochlorides by the reaction of N-phenyl-S-chloroisothiocarbamoyl chloride and N-glucosyl/lactosyl/maltosyl thiocarbamides is reported. The simple isolation method with good yields under mild condition is applicable for the present protocol. All the newly synthesized thiadiazolidin-3-thiones exhibit moderate to good antimicrobial activities against a variety of pathogen

Synthesis of some new carbohydrate-containing thiouriedonaphtho-quinones

Abstract New alkyl, aryl, and glycosylthiouriedo derivatives of 2,3-diamino-1,4-naphthoquinone were synthesized via the reaction of isothiocyanates with 2,3-diamino-1,4-naphthoquinone. The new compounds were fully characterized through their physicochemical properties.