6014-42-2

Basic information

• Product Name: 6-DEOXY-L-MANNOSE MONOHYDRATE
• Synonyms: L-(+)-RHAMNOSE HYDRATE;L-RHA H2O;L-(+)-RHAMMNOSE MONOHYDRATE;L-(+)-RHAMNOPYRANOSE, MONOHYDRATE;L-(+)-RHAMNOSE;ISODULCIT;ISODULCIT MONOHYDRATE;6-DEOXY-L-MANNOSE HYDRATE
• CAS NO: 6014-42-2
• Molecular Formula: C₆H₁₂O₅
• Molecular Weight: 182.17
• Mol File: 6014-42-2.mol
• Article Data: 104

Chemical Properties

• Melting Point: 91-93 °C
• Boiling Point: 323.9±42.0 °C(Predicted)
• Appearance: /
• Density: 1.556±0.06 g/cm3(Predicted)
• PKA: 12.28±0.70(Predicted)
• CAS DataBase Reference: 6-DEOXY-L-MANNOSE MONOHYDRATE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-DEOXY-L-MANNOSE MONOHYDRATE(6014-42-2)
• EPA Substance Registry System: 6-DEOXY-L-MANNOSE MONOHYDRATE(6014-42-2)

Safety Data

• Safety Statements: 24/25
• Hazardous Substances Data: 6014-42-2(Hazardous Substances Data)

Usage

Definition

ChEBI: An L-rhamnopyranose having alpha-configuration at the anomeric centre.

Upstream product

• 87425-35-2 (25S)-spirost-5-ene-1β,3β-diol 1-O- 2)-β-D-fucopyranoside> 
• 87425-34-1 (25S)-spirost-5-ene-1β,3β-diol 1-O-β-D-fucopyranoside 3-O-α-L-rhamnopyranoside 
• 143663-04-1 nolinofuroside F 22-O-methyl ether 
• 90985-63-0 β-3,4-trihydroxyphenethyl-O-α-L-rhamnopyranosyl-(1<*>3)-4-O-caffeoyl-β-D-glucopyranoside 
• 118525-35-2 sagittatoside A 
• 79852-10-1 Haplogenin 7-O-<6-O-acetyl-2-O-α-L-rhamnopyranosyl-β-D-glucopyranoside>, Haploside D 
• 55916-50-2 (25R)-26-O-β-D-glucopyranosyl-22-O-methylfurost-5-ene-3β,22ξ,26-triol 3-O-2)-O-β-D-glucopyranoside> 
• 91528-40-4 dauroside C 
• 75799-17-6 oleanolic acid 3-O-β-D-ribopyranosyl-(1-3)-α-L-rhamnopyranosyl-(1-2)-α-L-arabinopyranoside 
• 75799-17-6 oleanolic acid 3-O-β-D-xylopyranosyl-(1-3)-α-L-rhamnopyranosyl-(1-2)-α-L-arabinopyranoside 
• 75799-17-6 saponin V 
• 75799-17-6 hishoushi-saponin A 
• 522-12-3 quercitrin 
• 482-38-2 kaempferitrin 

Downstream Products

• 620-02-0 5-Methylfurfural 
• 822-36-6 4-methyl-1H-imidazole 
• 930-62-1 2,4-Dimethylimidazole 
• 20246-37-1 L-rhamnonic acid 
• 6336-63-6 rhamnose oxime 
• 488-31-3 L-arabinaric acid 
• 110-15-6 succinic acid 
• 513-86-0 3-hydroxy-2-butanon 
• 75-07-0 acetaldehyde 
• 78-98-8 2-oxopropanal 
• 513-85-9 2.3-butanediol 
• 42927-37-7 6-deoxy-talose-(methyl-phenyl-hydrazone) 
• 100300-50-3 rhamnose-phenylbenzylhydrazone 
• 14479-23-3 N-phenyl-rhamnopyranosylamine 

Relevant articles and documents

New triterpenoids from the red sea sponge Siphonochalina siphonella

Clear differences were found when comparing the chemical content of the northern, Gulf of Eilat, to the southern-central, Dahlak archipelago, Red Sea sponge Siphonochalina siphonella. The Dahlak sponge was found to be richer in the more polar triterpenes. Nine new compounds (1-4, 7, 8, 15-17) were isolated and identified, among them two sipholane glycosides, sipholenoside A and B (7 and 8), and one compound, dahabinone A (17), possessing a new skeleton.

New triterpenoid saponin from the stems of Albizia adianthifolia (Schumach.) W.Wight

As part of our continuing study of apoptosis-inducing saponins from Cameroonian Albizia genus, one new triterpenoid saponin, named adianthifolioside J (1), together with the known gummiferaoside E (2), were isolated from Albizia adianthifolia stems. The s

Oleanane-type saponins and prosapogenins from Albizia julibrissin and their cytotoxic activities

Two undescribed oleanane-type saponins, julibrosides K–L, along with three undescribed oleanane-type prosapogenins, julibrosides M–O, were isolated from the stem bark of Albizia julibrissin Durazz. and the mild alkaline hydrolysate of the total saponin, r