Cas 112380-08-2,1-Pyrrolidinecarboxylic acid, 2-[[(1-carboxycyclopentyl)amino]carbonyl]-, mono(1,1-dimethylethyl) ester, (S)-, compd. with N-cyclohexylcyclohexanamine (1:1)

112380-08-2

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Basic information

Product Name: 1-Pyrrolidinecarboxylic acid, 2-[[(1-carboxycyclopentyl)amino]carbonyl]-, mono(1,1-dimethylethyl) ester, (S)-, compd. with N-cyclohexylcyclohexanamine (1:1)
Synonyms:
CAS NO:112380-08-2
Molecular Formula: C16H26N2O5.C12H23N
Molecular Weight: 507.714
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-Pyrrolidinecarboxylic acid, 2-[[(1-carboxycyclopentyl)amino]carbonyl]-, mono(1,1-dimethylethyl) ester, (S)-, compd. with N-cyclohexylcyclohexanamine (1:1)(CAS DataBase Reference)
NIST Chemistry Reference: 1-Pyrrolidinecarboxylic acid, 2-[[(1-carboxycyclopentyl)amino]carbonyl]-, mono(1,1-dimethylethyl) ester, (S)-, compd. with N-cyclohexylcyclohexanamine (1:1)(112380-08-2)
EPA Substance Registry System: 1-Pyrrolidinecarboxylic acid, 2-[[(1-carboxycyclopentyl)amino]carbonyl]-, mono(1,1-dimethylethyl) ester, (S)-, compd. with N-cyclohexylcyclohexanamine (1:1)(112380-08-2)

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: 112380-08-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112380-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,3,8 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112380-08:
(8*1)+(7*1)+(6*2)+(5*3)+(4*8)+(3*0)+(2*0)+(1*8)=82
82 % 10 = 2
So 112380-08-2 is a valid CAS Registry Number.

112380-08-2Upstream product

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112380-08-2Relevant academic research and scientific papers

OXYTOCIN ANALOGUES WITH NON-CODED AMINO ACID RESIDUES IN POSITION 8:OXYTOCIN AND OXYTOCIN

Hlavacek, Jan,Pospisek, Jan,Slaninova, Jirina,Chan, Walter Y.,Hruby, Victor J.

, p. 2317 - 2325 (2007/10/02)

oxytocin (II) and oxytocin (III) were prepared by a combination of solid-phase synthesis and fragment condensation.Both analogues exhibited decreased uterotonic potency in vitro, each being about 15-30percent that of ox

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