CAS 83-87-4

D-Glucopiranose,1,2,3,4,6-pentaacetato

Descrição:

D-Glucopiranose, 1,2,3,4,6-pentaacetato é um derivado da D-glicose, onde todos os cinco grupos hidroxila são acetilados, resultando em um açúcar totalmente acetilado. Este composto é caracterizado por sua estrutura molecular, que inclui um anel de pirano, uma forma cíclica de seis membros da glicose, e cinco grupos acetila ligados às posições hidroxila. A acetilação aumenta a lipofilicidade da molécula, tornando-a menos polar em comparação com seu açúcar pai, o que pode influenciar sua solubilidade e reatividade. O pentaacetato de D-glucopiranose é tipicamente um sólido cristalino branco a off-white, e é solúvel em solventes orgânicos como clorofórmio e acetona, mas menos solúvel em água devido à presença dos volumosos grupos acetila. Este composto é frequentemente utilizado em síntese orgânica e como um intermediário na preparação de vários glicosídeos e outros derivados de carboidratos. Além disso, pode servir como um composto modelo em estudos relacionados à química de carboidratos e reações enzimáticas envolvendo glicosilação.

Fórmula: C₁₆H₂₂O₁₁

InChI: InChI=1S/C16H22O11/c1-7(17)22-6-12-13(23-8(2)18)14(24-9(3)19)15(25-10(4)20)16(27-12)26-11(5)21/h12-16H,6H2,1-5H3/t12-,13-,14+,15-,16?/m1/s1

Chave InChI: InChIKey=LPTITAGPBXDDGR-IWQYDBTJSA-N

SMILES: O(C(C)=O)[C@H]1[C@H](OC(C)=O)[C@@H](COC(C)=O)OC(OC(C)=O)[C@@H]1OC(C)=O

Sinónimos:

• 1,2,3,4,6-Penta-O-acetyl-<span class="text-smallcaps">D</span>-glucopyranose
• 1,2,3,4,6-Penta-O-acetyl-D-glucopyranose
• <span class="text-smallcaps">D</span>-Glucopyranose, 1,2,3,4,6-pentaacetate
• <span class="text-smallcaps">D</span>-Glucopyranose, pentaacetate
• <span class="text-smallcaps">D</span>-Glucose pentaacetate
• <span class="text-smallcaps">D</span>-Glucose, 1,2,3,4,6-pentaacetate
• D-Glucopyranose,pentaacetate (9CI)
• D-Glucose, 1,2,3,4,6-pentaacetate (7CI)
• D-Glucosepentaacetate
• Glucopyranose pentaacetate
• Glucopyranose, pentaacetate, <span class="text-smallcaps">D</span>-
• Glucopyranose,pentaacetate, D- (6CI,8CI)
• Glucose pentaacetate
• Pagosten-1
• Penta-O-acetyl-<span class="text-smallcaps">D</span>-glucopyranose
• Penta-O-acetyl-<span class="text-smallcaps">D</span>-glucopyranoside
• Penta-O-acetyl-D-glucopyranose
• Pentaacetyl-<span class="text-smallcaps">D</span>-glucose
• Pentaacetyl-D-glucose
• Pentaacetylglucose
• Peracetyl-<span class="text-smallcaps">D</span>-glucose
• Peracetyl-D-glucose
• Peracetylated <span class="text-smallcaps">D</span>-glucose
• D-Glucopyranose, 1,2,3,4,6-pentaacetate
• D-Glucopyranose, pentaacetate
• Glucopyranose, pentaacetate, D-
• D-Glucose, 1,2,3,4,6-pentaacetate
• Acetyl 2,3,4,6-tetra-o-acetyl-beta-D-glucopyranoside
• PENTA-O-ACETYL-BETA-D-GLUCOPYRANOSE
• GLUCOSE PENTAACETATE, B-D-
• PENTA-O-ACETYL-BETA-D-GLUCOPYRANOSIDE
• BETA-D(+)-GLUCOSE PENTAACETATE
• 1,2,3,4,6-PENTA-O-ACETYL-BETA-D-GLUCOSE
• BETA-D-GLUCOSE PENTAACETATE
• D-B-GLUCOSE PENTAACETATE
• 1,2,3,4,6-PENTAACETYL-ALPHA-D-GLUCOSE
• BETA-D-GLUCOPYRANOSE-PENTAACETATE
• B-D-1,2,3,4,6-PENTA-O-ACETYL-B-GLUCOPYRANOSE
• PENTAACETYL-BETA-D-GLUCOSE
• B-D-GLUCOSE PENTAACETATE
• 1,2,3,4,6-PENTA-O-ACETYL-BETA-D-GLUCOPYRANOSE
• BETA-DEXTROSE PENTAACETATE

(3R,4S,5R,6R)-6-(Acetoxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate

CAS: 83-87-4

Fórmula: C₁₆H₂₂O₁₁

Pureza: 95%

Cor e Forma: Solid

Peso molecular: 390.3393

Ref: IN-DA008HUJ

D-Glucose pentaacetate

CAS: 83-87-4

D-Glucose pentaacetate

Pureza: 98%

Ref: 54-OR1037877

1,2,3,4,6-Penta-O-acetyl-D-glucopyranose

CAS: 83-87-4

Ref: 7W-GC2521

Peracetylated D-glucose

CAS: 83-87-4

Pureza: 98%

Peso molecular: 390.341

Ref: 10-F986473

1,2,3,4,6-Penta-O-acetyl-D-glucopyranose

CAS: 83-87-4

Benzoate is a carboxylic acid that is found in many fruits and vegetables. Benzoate can be metabolized by the body to form hydrogen chloride, which may cause irritation of the mucous membranes of the respiratory tract. This chemical has been shown to have cytotoxic activity against human cancer cells in vitro. Benzoate also has an anti-inflammatory effect on insulin resistance and can be used as a topical treatment for psoriasis. The mechanism by which benzoate exerts its anticancer activity is not fully understood, but it may involve the production of reactive oxygen species or induction of apoptosis.

Fórmula: C₁₆H₂₂O₁₁

Pureza: Min. 95%

Cor e Forma: White Powder

Peso molecular: 390.34 g/mol

Ref: 3D-MP05825

α,β-D-Glucose pentaacetate

CAS: 83-87-4

Glucose pentaacetate is a form of glucose that reacts with boron trifluoride etherate to produce anomers. This process can be used to synthesize the anomeric form of glucose, which is important for the biosynthesis of glycosides. Glucose pentaacetate has been shown to react with nitrate and trifluoride, forming conjugates with aluminum and chloride. The catalytic stereocontrol of this reaction allows for the production of disaccharides without hydrogen chloride or formylation.

Fórmula: C₁₆H₂₂O₁₁

Peso molecular: 390.35 g/mol

Ref: 3D-G-2990