Best price 6-Deoxy-D-glucose CAS 7658-08-4 with high purity Company profile Wuhan Fortuna Chemical Co.,Ltd established in 2006, is a big integrative chemical enterprise being engaged in Pharmaceutical & its intermediates, Food/Feed additives
Cas:7658-08-4
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Cas:7658-08-4
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Cas:7658-08-4
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Cas:7658-08-4
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Cas:7658-08-4
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Cas:7658-08-4
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Cas:7658-08-4
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inquiry1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
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Cas:7658-08-4
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inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
We are committed to providing our customers with the best products and services at the most competitive prices.Appearance:yellowis to white powder Storage:Room temperature with sealed well Package:according to the clients requirement Application:Use
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United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat
FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the 6-DEOXY-D-GLUCOSE, CAS:7658-08-4 with the most competitive price and the best quality
D-Glucose, 6-deoxy-Appearance:Off white to slight yellow solid Storage:Store in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/Pharmaceutical intermediates Transportation:By Sea,by Air,By courier li
6-Deoxy-D-glucose;6-Deoxyglucose; D-6-Deoxyglucose; D-Chinovose; D-Isorhamnose; D-Quinovose;Epirhamnose, D-; Glucomethylose; Isorhamnose; Isorhodeose;…
Conditions | Yield |
---|---|
Stage #1: bayogenin {28-O-α-L-rhamnopyranosyl-(1->2)-[β-D-galactopyranosyl(1->3)]-[β-D-glucopyranosyl-(1->6)]-β-D-glucopyranosyl} ester With sulfuric acid In 1,4-dioxane for 1h; Reflux; Stage #2: In 1,4-dioxane | A n/a B n/a C n/a D 71.7% |
Conditions | Yield |
---|---|
Stage #1: desacylperennisoside X With sulfuric acid In 1,4-dioxane for 1h; Reflux; Stage #2: In 1,4-dioxane | A n/a B n/a C 65.8% |
Conditions | Yield |
---|---|
Stage #1: desacylperennisoside XI With sulfuric acid In 1,4-dioxane for 1h; Reflux; Stage #2: In 1,4-dioxane | A n/a B n/a C n/a D 61.4% |
Conditions | Yield |
---|---|
Stage #1: desacyl-perennisoside VIII With sulfuric acid In 1,4-dioxane for 1h; Reflux; Stage #2: In 1,4-dioxane | A n/a B n/a C n/a D 52.2% |
Conditions | Yield |
---|---|
Stage #1: desacylperennisoside IX With sulfuric acid In 1,4-dioxane for 1h; Reflux; Stage #2: In 1,4-dioxane | A n/a B n/a C n/a D n/a E 50% |
γ lactone of d-isorhamnonic acid
D-quionovose
D-quionovose
Conditions | Yield |
---|---|
Hydrolysis; |
D-quionovose
Conditions | Yield |
---|---|
With hydrogenchloride |
D-quionovose
Conditions | Yield |
---|---|
With sulfuric acid |
D-quionovose
Conditions | Yield |
---|---|
Hydrolysis; |
Conditions | Yield |
---|---|
With water; trifluoroacetic acid at 100℃; for 0.5h; |
Conditions | Yield |
---|---|
With water; trifluoroacetic acid at 100℃; for 0.5h; |
3-O-[3-O-methyl-β-D-glucopyranosyl-(1->3)-β-D-glucopyranosyl-(1->4)-β-D-quinovopyranosyl-(1->2)-4-O-sodiumsulfato-β-D-xylopyranosyl]-22-oxo-9(11)-holostene-3β,12α,17α-triol
A
D-xylose
B
D-quionovose
C
3-O-methyl-D-xylose
D
D-glucose
Conditions | Yield |
---|---|
With water; trifluoroacetic acid at 120℃; for 2h; |
3-O-[3-O-methyl-β-D-glucopyranosyl-(1->3)-β-D-glucopyranosyl-(1->4)-β-D-quinovopyranosyl-(1->2)-4-O-sodiumsulfato-β-D-xylopyranosyl]-22-oxo-9(11)-holostene-3β,12α,25-triol
A
D-xylose
B
D-quionovose
C
3-O-methyl-D-xylose
D
D-glucose
Conditions | Yield |
---|---|
With water; trifluoroacetic acid at 120℃; for 2h; |
fuscocineroside B
A
D-xylose
B
D-quionovose
C
3-O-methyl-D-xylose
D
D-glucose
Conditions | Yield |
---|---|
With water; trifluoroacetic acid at 120℃; for 2h; |
Conditions | Yield |
---|---|
With water; trifluoroacetic acid at 120℃; for 2h; |
Conditions | Yield |
---|---|
With water; trifluoroacetic acid at 120℃; for 2h; |
A
D-quionovose
B
L-Rhamnose
C
D-glucose
D
11-hydroxyhexadecanoic acid
Conditions | Yield |
---|---|
With hydrogenchloride; water In ethanol for 1h; Reflux; |
Conditions | Yield |
---|---|
With β-D-glucosidase at 37℃; for 6h; pH=5; aq. acetate buffer; Enzymatic reaction; | A 0.9 mg B 1.2 mg |
A
D-xylose
B
D-apiose
C
D-quionovose
D
L-Rhamnose
E
D-glucose
Conditions | Yield |
---|---|
With hydrogenchloride In 1,4-dioxane; water at 100℃; for 3h; |
Conditions | Yield |
---|---|
With hydrogenchloride; water at 95℃; for 1h; |
(3S,11S)-ipurolic acid 11-O-β-D-quinovopyranosyl-(1->2)-O-β-D-glucopyranosyl-(1->3)-[O-β-D-quinovopyranosyl-(1->4)]-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-glucopyranosyl-(1->2)-β-D-fucopyranoside
A
D-quionovose
B
D-Fucose
C
L-Rhamnose
D
D-glucose
Conditions | Yield |
---|---|
With hydrogenchloride; water at 95℃; for 1h; |
(3S,11S)-ipurolic acid 11-O-β-D-quinovopyranosyl-(1->2)-O-β-D-glucopyranosyl-(1->3)-[O-β-D-fucopyranosyl-(1->4)]-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-glucopyranosyl-(1->2)-β-D-fucopyranoside
A
D-quionovose
B
D-Fucose
C
L-Rhamnose
D
D-glucose
Conditions | Yield |
---|---|
With hydrogenchloride; water at 95℃; for 1h; |
(3S,11S)-ipurolic acid 11-O-β-D-fucoopyranosyl-(1->3)-O-β-D-quinovopyranosyl-(1->2)-O-β-D-glucopyranosyl-(1->3)-[O-β-D-fucopyranosyl-(1->4)]-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-glucopyranosyl-(1->2)-β-D-fucopyranoside
A
D-quionovose
B
D-Fucose
C
L-Rhamnose
D
D-glucose
Conditions | Yield |
---|---|
With hydrogenchloride; water at 95℃; for 1h; |
(3S,11S)-ipurolic acid 11-O-α-L-rhamnpyranosyl-(1->3)-O-β-D-quinovopyranosyl-(1->2)-O-β-D-glucopyranosyl-(1->3)-[O-β-D-quinovopyranosyl-(1->4)]-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-glucopyranosyl-(1->2)-β-D-fucopyranoside
A
D-quionovose
B
D-Fucose
C
L-Rhamnose
D
D-glucose
Conditions | Yield |
---|---|
With hydrogenchloride; water at 95℃; for 1h; |
Conditions | Yield |
---|---|
With hydrogenchloride; water In 1,4-dioxane at 100℃; for 1h; |
Conditions | Yield |
---|---|
With hydrogenchloride In 1,4-dioxane; water for 1h; Reflux; |
Conditions | Yield |
---|---|
With hydrogenchloride In 1,4-dioxane; water at 95℃; for 1h; Inert atmosphere; |
O-β-D-glucopyranosyl-(1->6)-β-D-glucopyranosyl 3-[(O-β-D-glucopyranosyl-(1->3)-O-[α-L-rhamnopyranosyl-(1->2)]-α-L-arabinopyranosyl)oxy]-30-noroleana-12,20(29)-dien-28-oate
A
L-arabinose
B
D-quionovose
C
D-glucose
Conditions | Yield |
---|---|
With hydrogenchloride In 1,4-dioxane; water at 95℃; for 1h; Inert atmosphere; |
D-quionovose
Conditions | Yield |
---|---|
With iodine; acetic acid | 78% |
Conditions | Yield |
---|---|
In methanol; dichloromethane at 40℃; for 48h; | 8% |
phenylhydrazine hydrochloride
arabino-6-deoxy-[2]hexosulose-bis-phenylhydrazone
Conditions | Yield |
---|---|
With ethanol; water; sodium acetate phenyl-isorhodeosazone; |
D-quionovose
6-deoxy-D-glucitol
Conditions | Yield |
---|---|
With sodium amalgam; sulfuric acid; water | |
With sodium tetrahydroborate |
D-quionovose
d-glucomethylonic acid
Conditions | Yield |
---|---|
With potassium hydroxide; platinum on activated charcoal In water at 25℃; under 760 Torr; for 1.5h; Rate constant; Mechanism; relative, initial rate; | |
With bromine |
D-quionovose
Conditions | Yield |
---|---|
With nitric acid at 50 - 55℃; |
D-quionovose
acetic anhydride
1,2,3,4-tetra-O-acetyl-6-deoxy-β-D-glucopyranose
Conditions | Yield |
---|---|
With sodium acetate |
Conditions | Yield |
---|---|
With sulfuric acid |
Conditions | Yield |
---|---|
With acetic acid -bis-<4-bromo-phenylhydrazone>; |
Conditions | Yield |
---|---|
With acetic acid |
N-benzyloxyamine
A
trifluoroacetylated 6-deoxyglucose anti-O-benzyloxime
B
trifluoroacetylated 6-deoxyglucose syn-O-benzyloxime
Conditions | Yield |
---|---|
1.) NMP, 75 deg C, 30 min, 2.) NMP, RT, 5-10 min; Multistep reaction; |
O-Methylhydroxylamin
D-quionovose
1-(Trimethylsilyl)imidazole
A
trimethylsilyl ether of 6-deoxyglucose anti-O-methyloxime
B
trimethylsilyl ether of 6-deoxyglucose syn-O-methyloxime
Conditions | Yield |
---|---|
1.) NMP, 75 deg C, 30 min, 2.) NMP, RT, 5-10 min; Multistep reaction; |
D-quionovose
N-benzyloxyamine
1-(Trimethylsilyl)imidazole
A
trimethylsilyl ether of 6-deoxyglucose-O-benzyloxime
B
trimethylsilyl ether of 6-deoxygalactose-anti-O-benzyloxime
Conditions | Yield |
---|---|
1.) NMP, 75 deg C, 30 min, 2.) NMP, RT, 5-10 min; Multistep reaction; |
Conditions | Yield |
---|---|
In water at 200℃; for 1h; Title compound not separated from byproducts; | |
In water at 200℃; for 1h; |
Conditions | Yield |
---|---|
at 50 - 55℃; |
Conditions | Yield |
---|---|
Stage #1: D-quionovose With dmap; hydroxylamine at 60℃; for 0.5h; Stage #2: acetic anhydride at 60℃; for 0.5h; |
D-quionovose
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sulfuric acid 2: silver carbonate; chloroform View Scheme |
D-quionovose
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: sulfuric acid 2: silver carbonate; chloroform 3: pyridine View Scheme |
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