Cas 1251002-01-3,tert-Butyl 8-oxa-2,5-diazaspiro[3.5]nonane-2-carboxylate

1251002-01-3

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Basic information

Product Name: tert-Butyl 8-oxa-2,5-diazaspiro[3.5]nonane-2-carboxylate
Synonyms: tert-Butyl 8-oxa-2,5-diazaspiro[3.5]nonane-2-carboxylate;8-Oxa-2,5-Diaza-Spiro[3.5]Nonane-2-Carboxylicacidtert-Butylester;2-Boc-8-oxa-2,5-diaza-spiro[3.5]nonane
CAS NO:1251002-01-3
Molecular Formula: C11H20N2O3
Molecular Weight: 228.2881
EINECS: N/A
Product Categories: N/A
Mol File: 1251002-01-3.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 330.9±42.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 1.15±0.1 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 7.83±0.20(Predicted)
CAS DataBase Reference: tert-Butyl 8-oxa-2,5-diazaspiro[3.5]nonane-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-Butyl 8-oxa-2,5-diazaspiro[3.5]nonane-2-carboxylate(1251002-01-3)
EPA Substance Registry System: tert-Butyl 8-oxa-2,5-diazaspiro[3.5]nonane-2-carboxylate(1251002-01-3)

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: 1251002-01-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1251002-01-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,1,0,0 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1251002-01:
(9*1)+(8*2)+(7*5)+(6*1)+(5*0)+(4*0)+(3*2)+(2*0)+(1*1)=73
73 % 10 = 3
So 1251002-01-3 is a valid CAS Registry Number.

1251002-01-3Upstream product

398489-26-4 tert-butyl 3-oxoazetidine-1-carboxylate

1251002-01-3Downstream Products

1251002-01-3Relevant academic research and scientific papers

One-step synthesis of saturated spirocyclic N-heterocycles with stannyl amine protocol (SnAP) reagents and ketones

Siau, Woon-Yew,Bode, Jeffrey W.

supporting information, p. 17726 - 17729 (2015/02/19)

The combination of cyclic ketones and stannyl amine protocol (SnAP) reagents affords saturated, spirocyclic N-heterocycles under operationally simple reaction conditions. The resulting, N-unprotected spirocyclic amines are in great demand as scaffolds for

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