4753-07-5

4753-07-5 structure

Name: Bromo Heptaacetyl-D-lactoside
Chemical Name: Bromo Heptaacetyl-D-lactoside
CAS Number: 4753-07-5
Molecular Formula: C₂₆H₃₅BrO₁₇
Molecular Weight: 699.45000
Create Date: 2016-10-18 16:29:39
Modify Date: 2026-10-11 19:25:21

Name	Bromo Heptaacetyl-D-lactoside
Synonyms	2,3,6,2',3',4',6'-Hta-O-acetyl-1-bromo-1-deoxy-alpha-D-lactopyranose min Acetobromo-a-D-lactoside AcetobroMo-α-D-lactoside, BroMo 4-O-(2 ,3,4,6-tetra-O-acetyl- β-D-galactopyranosyl) -2,3,6-tri-O-acetyl-α -D-glucopyranoside Hta-O-acetyl-α- D -lactosyl bromide Hta-O-acetyl-α-D-lactosyl Bromide Acetobromo-alpha-D-lactose, 2,3,6,2',3',4',6'-Hta-O-acetyl-alpha-D-lactosyl bromide, alpha-D-Lactosyl bromide htaacetate (2R,3S,4S,5R,6S)-2-(acetoxymethyl)-6-(((2R,3R,4S,5R,6R)-4,5-diacetoxy-2-(acetoxymethyl)-6-bromotetrahydro-2H-pyran-3-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate α-D-Glucopyranosyl bromide, 4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-, 2,3,6-triacetate 2,3,6,2',3',4',6'-Hta-O-acetyl-a-D-lactosyl bromide BROMO 4-O-(2,3,4,6-TETRA-O-ACETYL- BETA-D-GALACTOPYRANOSYL)-2,3,6-TRI-O-ACETYL-ALPHA-D-GLUCOPYRANOSIDE ACETYLATED LACTOSE BROMIDE 2,2',3,3',4',6,6'-Hta-O-acetyl-α-D-lactosyl bromide ACETOBROMOLACTOSE BROMO HTAACETYL-D-LACTOSIDE ACETOBROMO-ALPHA-D-LACTOSIDE alpha.-D-Glucopyranosyl bromide, 4-O-(2,3,4,6-tetra-O-acetyl-.beta.-D-galactopyranosyl)-, triacetate 2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTOPYRANOSYL-2,3,6-TRI-O-ACETYL-ALPHA-D-GLUCOPYRANOSYL BROMIDE ACETOBROMO-ALPHA-D-LACTOSE 2,3,6,2',3',4',6'-Hta-O-acetyl-alpha-D-lactosyl bromide 2,3,6,2',3',4',6'-Hta-O-acetyl-1-bromo-1-deoxy-alpha-D-lactopyranose 2,2',3,3',4',6,6'-HTA-O-ACETYL-ALPHA-D-LACTOSYL BROMIDE [(2R,3S,4S,5R,6S)-3,4,5-triacetyloxy-6-[(2R,3R,4S,5R,6R)-4,5-diacetyloxy-2-(acetyloxymethyl)-6-bromooxan-3-yl]oxyoxan-2-yl]methyl acetate

Melting Point	140-141ºC
Molecular Formula	C₂₆H₃₅BrO₁₇
Molecular Weight	699.45000
Exact Mass	698.10600
PSA	211.79000
LogP	0.00100

3616-19-1

~98%

4753-07-5

Literature: Allen; Zhang; Williams; Zatorski; Ragupathi; Livingston; Danischefsky Chemistry - A European Journal, 2000 , vol. 6, # 8 p. 1366 - 1375

133-99-3

506-96-7

108-24-7

~96%

4753-07-5

Literature: Yang, Yang; Xue, Xiao-Chao; Jin, Xiao-Feng; Wang, Li-Jun; Sha, Yin-Lin; Li, Zhong-Jun Tetrahedron, 2012 , vol. 68, # 35 p. 7148 - 7154

133-99-3

108-24-7

~94%

4753-07-5

Literature: Yang, Yang; Cui, Xi-Kai; Zhong, Ming; Li, Zhong-Jun Carbohydrate Research, 2012 , vol. 361, p. 189 - 194

34213-32-6

~91%

4753-07-5

Literature: Seebacher, Werner; Weis, Robert; Jurenitsch, Johann; Rauchensteiner, Katharina; Haslinger, Ernst Monatshefte fur Chemie, 2000 , vol. 131, # 9 p. 985 - 996

18464-08-9

~79%

4753-07-5

Literature: Mani; Kanakamma Synthetic Communications, 1992 , vol. 22, # 15 p. 2175 - 2182

160227-12-3

~81%

4753-07-5

572-09-8

3068-32-4

Literature: Zhang, Zhiyuan; Magnusson, Goeran Carbohydrate Research, 1996 , vol. 295, p. 41 - 55

133-99-3

4753-07-5

Literature: Helvetica Chimica Acta, , vol. 92, # 1 p. 176 - 187

108-24-7

63-42-3

4753-07-5

Literature: Nature (London, United Kingdom), , vol. 165, p. 369

63-42-3

4753-07-5

Literature: E-Journal of Chemistry, , vol. 8, # 4 p. 1614 - 1619

Precursor 7
3616-19-1 133-99-3 506-96-7 108-24-7
34213-32-6 160227-12-3 63-42-3
DownStream 9
3616-19-1 17691-02-0 51450-24-9 84034-75-3
67310-53-6 69266-16-6 74513-17-0 53669-33-3
13223-83-1

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