N-4-Boc-aminocyclohexanone - ≥98% , CAS No.179321-49-4

CAS: 179321-49-4 Cat. No.: N134328 Molecular Weight: 213.27 EC Number: 672-405-6
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
(4-oxocyclohexyl)carbamic acid tert-butyl ester | N-4-Boc-aminocyclohexanone, AldrichCPR | (4-Oxocyclohexyl)carbamic acid tert-butyl ester;N-Boc-4-Aminocyclohexanone | AC-1691 | Z255149962 | AKOS004910703 | N-4-Boc-aminocyclohexanone, 95% | PS-5440 | N-4-
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
N134328-1g
3
$9.90
5g
N134328-5g
4
$10.90
25g
N134328-25g
2

$24.90

$37.90
Save $13.00 (34.30%)
100g
N134328-100g
1

$83.90

$125.90
Save $42.00 (33.36%)
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Product Application:
4-(N-Boc-amino)cyclohexanone is an intermediate in the synthesis of tert-Butyl 1,7-diazaspiro[3.5]nonane-1-carboxylate (B692795). tert-Butyl 1,7-diazaspiro[3.5]nonane-1-carboxylate is a reagent in the preparation of -[4-fluoro-3-(piperazin-1-ylcarbonyl)benzyl]-4,5-dimethylpyridazin-3(2H)-ones as a potent poly(ADP-ribose) polymerase-1 inhibitors active in BRCA deficient cells.

Specifications

Synonyms
(4-oxocyclohexyl)carbamic acid tert-butyl ester | N-4-Boc-aminocyclohexanone, AldrichCPR | (4-Oxocyclohexyl)carbamic acid tert-butyl ester;N-Boc-4-Aminocyclohexanone | AC-1691 | Z255149962 | AKOS004910703 | N-4-Boc-aminocyclohexanone, 95% | PS-5440 | N-4-
Specifications & Purity
≥98%
Storage
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98%
Names and Identifiers
Pubchem Sid504760541
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504760541
Canonical SmilesCC(C)(C)OC(=O)NC1CCC(=O)CC1
IUPAC Nametert-butyl N-(4-oxocyclohexyl)carbamate
InChIKeyWYVFPGFWUKBXPZ-UHFFFAOYSA-N
INCHI1S/C11H19NO3/c1-11(2,3)15-10(14)12-8-4-6-9(13)7-5-8/h8H,4-7H2,1-3H3,(H,12,14)
Isomeric SMILES CC(C)(C)OC(=O)NC1CCC(=O)CC1
WGK Germany 3
Molecular Weight 213.27
Reaxy-Rn 9326824
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9326824&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Carbamic acids and derivatives
Direct ParentCarbamate esters
Alternative Parents Organic carbonic acids and derivatives  Cyclic ketones  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic homomonocyclic compounds
Substituents Carbamic acid ester - Cyclic ketone - Carbonic acid derivative - Ketone - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as carbamate esters. These are compounds containing an ester of carbamic acid with the general structure R2NC(=O)OR' (R' not H). They are esters of carbamic acids.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot NumberCertificate TypeDateItem
I2308486Certificate of AnalysisJun 10, 2025 N134328
I2308488Certificate of AnalysisJun 10, 2025 N134328
I2308489Certificate of AnalysisJun 10, 2025 N134328
I2308551Certificate of AnalysisJun 10, 2025 N134328
F1529103Certificate of AnalysisOct 14, 2024 N134328
L2106695Certificate of AnalysisSep 19, 2023 N134328
L2107066Certificate of AnalysisSep 19, 2023 N134328
Chemical and Physical Properties
SolubilitySoluble in methanol
Melt Point(°C)114-118 °C
Molecular Weight213.270 g/mol
XLogP31.200
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count3
Exact Mass213.136 Da
Monoisotopic Mass213.136 Da
Topological Polar Surface Area55.400 Ų
Heavy Atom Count15
Formal Charge0
Complexity245.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Fang Chen, Li Yin, Teng He, Tao Chen, Hangbo Yue, Chufen Yang.  (2023)  Fabrication of Dual pH/Reduction-Responsive P(CL-co-ACL)-Based Cross-Linked Polymeric Micelles for PTX Delivery.  LANGMUIR,      [PMID:37934563] [10.1021/acs.langmuir.3c02077]
Solution Calculators
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