Cas 55097-10-4,1,5-Pentanediamine, N-(phenylmethyl)-

55097-10-4

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Basic information

Product Name: 1,5-Pentanediamine, N-(phenylmethyl)-
Synonyms:
CAS NO:55097-10-4
Molecular Formula: C12H20N2
Molecular Weight: 192.304
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1,5-Pentanediamine, N-(phenylmethyl)-(CAS DataBase Reference)
NIST Chemistry Reference: 1,5-Pentanediamine, N-(phenylmethyl)-(55097-10-4)
EPA Substance Registry System: 1,5-Pentanediamine, N-(phenylmethyl)-(55097-10-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 55097-10-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 55097-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,9 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55097-10:
(7*5)+(6*5)+(5*0)+(4*9)+(3*7)+(2*1)+(1*0)=124
124 % 10 = 4
So 55097-10-4 is a valid CAS Registry Number.

55097-10-4Upstream product

55097-10-4Downstream Products

444147-74-4 N-benzyl-N'-pyren-1-ylmethyl-1,5-diaminopentane

55097-10-4Relevant academic research and scientific papers

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

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Paragraph 0104; 0105; 0110; 0111, (2018/04/03)

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)

Modular fluorescence sensors for saccharides

Arimori, Susumu,Bell, Michael L.,Oh, Chan S.,Frimat, Karine A.,James, Tony D.

, p. 803 - 808 (2007/10/03)

Modular photoinduced electron transfer (PET) sensors bearing two phenylboronic acid groups, a pyrene group and alkylene linkers, from trimethylene to octamethylene, have been prepared and evaluated. The diboronic acid systems with tetramethylene 34 pentamethylene 35 and hexamethylene 36 linkers display the greatest enhancement in binding relative to monoboronic acid 4 with D-glucose. The diboronic acid system with the hexamethylene 36 linker is particularly D-glucose selective and sensitive. Whilst the diboronic acid systems with the longer heptamethylene 37 and octamethylene 38 linkers display the greatest enhancement in binding relative to monoboronic acid 4 with D-galactose. All saccharide titrations were performed in methanolic aqueous solution.

Fibrin stabilizing factor inhibitors. 12. 5 dibenzylaminopentylamine and related compounds, a new type of FSF inhibitors

Hoffmann,Stenberg,Ljunggren,Svensson,Nilsson

, p. 278 - 284 (2007/10/04)

A series of omega dibenzylaminoalkylamines and related compounds have been prepared and tested as inhibitors of fibrin cross linking. This structural type was chosen in an attempt to develop noncompetitive inhibitors of fibrinoligase. By the combination o

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