Cas 926895-32-1,2-<i>tert</i>-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-(1-isopropyl-2-methyl-propyl) ester

926895-32-1

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Basic information

Product Name: 2-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-(1-isopropyl-2-methyl-propyl) ester
Synonyms: 2-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-(1-isopropyl-2-methyl-propyl) ester
CAS NO:926895-32-1
Molecular Formula:
Molecular Weight: 435.561
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: 2-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-(1-isopropyl-2-methyl-propyl) ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-(1-isopropyl-2-methyl-propyl) ester(926895-32-1)
EPA Substance Registry System: 2-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-(1-isopropyl-2-methyl-propyl) ester(926895-32-1)

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: 926895-32-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 926895-32-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,6,8,9 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 926895-32:
(8*9)+(7*2)+(6*6)+(5*8)+(4*9)+(3*5)+(2*3)+(1*2)=221
221 % 10 = 1
So 926895-32-1 is a valid CAS Registry Number.

926895-32-1Upstream product

926895-32-1Downstream Products

915193-99-6 H-Glu[O-(2,4-dimethyl-3-pentyl)]-OBn

926895-32-1Relevant academic research and scientific papers

Inhibition of P-glycoprotein-mediated multidrug efflux by aminomethylene and ketomethylene analogs of reversins

Koubeissi, Ali,Raad, Imad,Ettouati, Laurent,Guilet, David,Dumontet, Charles,Paris, Joelle

, p. 5700 - 5703 (2006)

Several aminomethylene analogs and a ketomethylene analog of reversins were synthesized in order to evaluate their ability to inhibit P-glycoprotein-mediated drug efflux in K562/R7 human leukemic cells overexpressing P-glycoprotein. These analogs retained

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