25079-94-1

Basic information

• Product Name: 1,6-Hexanediamine, N-(phenylmethyl)-
• CAS NO: 25079-94-1
• Molecular Formula: C13H22N2
• Molecular Weight: 206.331
• Mol File: 25079-94-1.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 1,6-Hexanediamine, N-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,6-Hexanediamine, N-(phenylmethyl)-(25079-94-1)
• EPA Substance Registry System: 1,6-Hexanediamine, N-(phenylmethyl)-(25079-94-1)

Safety Data

• Hazardous Substances Data: 25079-94-1(Hazardous Substances Data)

Upstream product

• 124-09-4 1,6-Hexanediamine 
• 100-52-7 benzaldehyde 
• 100-44-7 benzyl chloride 
• 171348-08-6 N¹-[1-Phenyl-meth-(E)-ylidene]-hexane-1,6-diamine 
• 100-39-0 benzyl bromide 
• 103-67-3 benzyl-methyl-amine 

Downstream Products

• 474005-09-9 Fe(η5-C5H5)(η5-C5H4CH2NH(CH2)6NHCH2C6H5) 
• 578740-12-2 N-anthracen-9-ylmethyl-N'-benzyl-hexane-1,6-diamine 
• 578740-11-1 N-benzyl-N'-phenanthren-9-ylmethyl-hexane-1,6-diamine 
• 578740-13-3 N-benzyl-N'-naphthalen-1-ylmethyl-hexane-1,6-diamine 
• 578740-14-4 N-benzyl-N'-naphthalen-2-ylmethyl-hexane-1,6-diamine 
• 424821-51-2 N-benzyl-N'-pyren-1-ylmethyl-1,6-diaminohexane 

Relevant articles and documents

A new kind of acetylcholine esterase inhibitors and its preparation method and application (by machine translation)

The present invention provides a novel acetyl choline esterase inhibitor and its preparation method and application, in particular, the invention discloses a formula A shown with double AChE binding site of substituted acridine compound, and its preparation method and as acetylcholinesterase inhibitors. The preparation of the novel compounds of this invention demonstrate good inhibit acetylcholine esterase role, can be used as a preparation for treating and preventing HAMER (AD) application value. (by machine translation)

Olefin epoxidation with chiral salen Mn(iii) immobilized on ZnPS-PVPA upon alkyldiamine

The asymmetric epoxidation of unfunctionalized olefins using Jacobsen's catalyst is an effective strategy to achieve chiral epoxides. We report Jacobsen's catalysts anchored onto ZnPS-PVPA upon alkyldiamines as active heterogeneous catalysts for the epoxi

Electrochemical saccharide sensor

The invention provides compounds for detecting sacchharides by electrochemistry. The compounds have a structure that includes a first boronic acid group attached by a first linker group to a first tertiary amine. The first tertiary amine is attached to a reporter group that includes an organometalic reporter moiety. A spacer group attaches the first tertiary amine to a second tertiary amine. The second tertiary amine is attached to an R group and a second linker group. The second linker group is attached to a second boronic acid group. In preferred embodiments, the compound selectively detects glucose and has a higher relative stability constant for glucose than for other saccharides.