Boc-L-Aspartic acid 4-methyl ester - ≥98% , CAS No.59768-74-0

CAS: 59768-74-0 Cat. No.: B110962 Molecular Weight: 247.25 Beilstein Registry Number: 4810472 EC Number: 818-022-1
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
AC-8612 | Boc-Asp(OMe)-OH, >=98.0% (TLC) | DTXSID20450548 | HY-W007399 | (2S)-2-{[(tert-butoxy)carbonyl]amino}-4-methoxy-4-oxobutanoic acid | EN300-199052 | (S)-2-(tert-butoxycarbonylamino)-4-methoxy-4-oxobutanoic acid | Boc-Asp(OMe)-OH | AKOS010365904 |
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
B110962-1g
4
$9.90
5g
B110962-5g
3
$10.90
10g
B110962-10g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$11.90
25g
B110962-25g
3

$26.90

$40.90
Save $14.00 (34.23%)
100g
B110962-100g
4

$106.90

$160.90
Save $54.00 (33.56%)
500g
B110962-500g
1

$533.90

$800.90
Save $267.00 (33.34%)
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Why this grade

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

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Storage & shipping

Room temperature Ships Normal 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.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
AC-8612 | Boc-Asp(OMe)-OH, >=98.0% (TLC) | DTXSID20450548 | HY-W007399 | (2S)-2-{[(tert-butoxy)carbonyl]amino}-4-methoxy-4-oxobutanoic acid | EN300-199052 | (S)-2-(tert-butoxycarbonylamino)-4-methoxy-4-oxobutanoic acid | Boc-Asp(OMe)-OH | AKOS010365904 |
Specifications & Purity
≥98%
Storage
Room temperature
Shipped In
Normal
Purity
≥98%
Names and Identifiers
Pubchem Sid488197014
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488197014
Canonical SmilesCC(C)(C)OC(=O)NC(CC(=O)OC)C(=O)O
IUPAC Name(2S)-4-methoxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoic acid
InChIKeyWFPSMPYVXFVVFA-LURJTMIESA-N
INCHI1S/C10H17NO6/c1-10(2,3)17-9(15)11-6(8(13)14)5-7(12)16-4/h6H,5H2,1-4H3,(H,11,15)(H,13,14)/t6-/m0/s1
Isomeric SMILES CC(C)(C)OC(=O)N[C@@H](CC(=O)OC)C(=O)O
WGK Germany 3
Molecular Weight 247.25
Beilstein 4810472
Reaxy-Rn 8980865
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8980865&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 - Alpha amino acids and derivatives
Direct ParentAspartic acid and derivatives
Alternative Parents Fatty acid methyl esters  Branched fatty acids  Dicarboxylic acids and derivatives  Methyl esters  Carbamate esters  Carboxylic acids  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Aspartic acid or derivatives - Branched fatty acid - Fatty acid ester - Fatty acid methyl ester - Dicarboxylic acid or derivatives - Fatty acyl - Methyl ester - Carbamic acid ester - Carboxylic acid ester - Carboxylic acid - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Organooxygen compound - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as aspartic acid and derivatives. These are compounds containing an aspartic acid or a derivative thereof resulting from reaction of aspartic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





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.

12 results found

Lot NumberCertificate TypeDateItem
C2630155Certificate of AnalysisApr 15, 2026 B110962
C2307026Certificate of AnalysisDec 17, 2022 B110962
C2307029Certificate of AnalysisDec 17, 2022 B110962
C2307031Certificate of AnalysisDec 17, 2022 B110962
C2307313Certificate of AnalysisDec 17, 2022 B110962
C2307314Certificate of AnalysisDec 17, 2022 B110962
C2307315Certificate of AnalysisDec 17, 2022 B110962
C2307325Certificate of AnalysisDec 17, 2022 B110962
C2307345Certificate of AnalysisDec 17, 2022 B110962
C2307347Certificate of AnalysisDec 17, 2022 B110962
E2325146Certificate of AnalysisDec 17, 2022 B110962
H2525025Certificate of AnalysisDec 17, 2022 B110962

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Chemical and Physical Properties
Molecular Weight247.240 g/mol
XLogP30.400
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count6
Rotatable Bond Count7
Exact Mass247.106 Da
Monoisotopic Mass247.106 Da
Topological Polar Surface Area102.000 Ų
Heavy Atom Count17
Formal Charge0
Complexity306.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Solution Calculators
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