527-22-0

Basic information

• Product Name: 6c-amino-cyclohexane-1r,2t,3c,4t,5c-pentaol
• Synonyms: 6c-amino-cyclohexane-1r,2t,3c,4t,5c-pentaol
• CAS NO: 527-22-0
• Molecular Weight: 179.173
• Mol File: 527-22-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 6c-amino-cyclohexane-1r,2t,3c,4t,5c-pentaol(CAS DataBase Reference)
• NIST Chemistry Reference: 6c-amino-cyclohexane-1r,2t,3c,4t,5c-pentaol(527-22-0)
• EPA Substance Registry System: 6c-amino-cyclohexane-1r,2t,3c,4t,5c-pentaol(527-22-0)

Safety Data

• Hazardous Substances Data: 527-22-0(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 7045-48-9 myo-inosose-⁽²⁾-phenylhydrazone 
• 7664-41-7 ammonia 
• 18391-54-3 1D-O³,O⁴;O⁵,O⁶-diisopropyliden-1,2-anhydro-allo-inositol 
• 6556-12-3 D-glucuronic acid 
• 4969-30-6 (2R,3R,4S,6R)-6-Nitro-cyclohexane-1,2,3,4,5-pentaol 
• 22263-78-1 D-myo-Inosose-⁽¹⁾-phenylhydrazon; (-)-vibo-Inosose-phenylhydrazon 
• 7045-47-8 (+/-)-epi-inosose-⁽²⁾-phenylhydrazone 

Downstream Products

• 64938-54-1 1D-penta-O-acetyl-1-acetylamino-1-deoxy-myo-inositol 
• 7011-06-5 penta-O-acetyl-1-acetylamino-1-deoxy-scyllo-inositol 
• 20097-49-8 penta-O-acetyl-3-acetylamino-3-deoxy-muco-inositol 
• 3613-86-3 N-Acetyl-muco-inosamin-⁽³⁾ 
• 3613-86-3 1-acetylamino-1-deoxy-scyllo-inositol 
• 3613-86-3 N-acetyl-myo-inosamine 
• 2772-86-3 DL-penta-O-acetyl-2-acetylamino-2-deoxy-epi-inositol 
• 2772-86-3 DL-penta-O-acetyl-4-acetylamino-4-deoxy-myo-inositol 
• 77123-07-0 N-acetylaminocyclitol pentaacetate 
• 22144-52-1 (+/-)-3r,4t,5c-trihydroxy-cyclohexane-1,2-dione-bis-phenylhydrazone 
• 19046-72-1 penta-O-acetyl-2-acetylamino-2-deoxy-myo-inositol 
• 3613-86-3 2-acetylamino-2-deoxy-myo-inositol 
• 488-73-3 (+/-)-cyclohexane-1r,2c,3t,4c,5t-pentaol 
• 117472-21-6 2-dimethylamino-2-deoxy-myo-inositol; hydrochloride 

Relevant articles and documents

Small-scale one-pot reductive alkylation of unprotected aminocyclitols with supported reagents

A protocol for the reductive alkylation of unprotected aminocyclitols with supported reagents and scavengers is described. The method is operatively simple and provides the corresponding secondary amines in high yields and purities. Georg Thieme Verlag Stuttgart.