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40248-63-3 molecular structure
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2-{[(1R,2S,5R)-5-methyl-2-(propan-2-yl)cyclohexyl]oxy}acetic acid

ChemBase ID: 109931
Molecular Formular: C12H22O3
Molecular Mass: 214.30128
Monoisotopic Mass: 214.15689456
SMILES and InChIs

SMILES:
CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OCC(=O)O
Canonical SMILES:
C[C@@H]1CC[C@H]([C@@H](C1)OCC(=O)O)C(C)C
InChI:
InChI=1S/C12H22O3/c1-8(2)10-5-4-9(3)6-11(10)15-7-12(13)14/h8-11H,4-7H2,1-3H3,(H,13,14)/t9-,10+,11-/m1/s1
InChIKey:
CILPHQCEVYJUDN-OUAUKWLOSA-N

Cite this record

CBID:109931 http://www.chembase.cn/molecule-109931.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
2-{[(1R,2S,5R)-5-methyl-2-(propan-2-yl)cyclohexyl]oxy}acetic acid
IUPAC Traditional name
{[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxy}acetic acid
Synonyms
(-)-Menthyl carboxymethyl ether
(-)-Menthyloxyacetic acid
L-MENTHOXYACETIC ACID
(-)-薄荷基羧甲基醚
(-)-薄荷氧基乙酸
CAS Number
40248-63-3
EC Number
254-857-2
MDL Number
MFCD00001483
Beilstein Number
2444474
PubChem SID
162095531
24896607
PubChem CID
7018861

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
PubChem 7018861 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 4.499642  H Acceptors
H Donor LogD (pH = 5.5) 1.744947 
LogD (pH = 7.4) -0.02388805  Log P 2.785383 
Molar Refractivity 58.2811 cm3 Polarizability 23.31536 Å3
Polar Surface Area 46.53 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Apperance
yellow liquid expand Show data source
Melting Point
52-55 °C(lit.) expand Show data source
Boiling Point
163-164 °C/10 mmHg(lit.) expand Show data source
Flash Point
113 °C expand Show data source
235.4 °F expand Show data source
Density
1.01 g/mL at 20 °C(lit.) expand Show data source
Refractive Index
n20/D 1.4672(lit.) expand Show data source
Optical Rotation
[α]20/D -93±3°, c = 10% in ethanol expand Show data source
[α]25/D -92.5°, c = 4 in methanol expand Show data source
European Hazard Symbols
Irritant Irritant (Xi) expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
Download expand Show data source
German water hazard class
3 expand Show data source
Risk Statements
36/37/38 expand Show data source
Safety Statements
26-36 expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H315-H319-H335 expand Show data source
GHS Precautionary statements
P261-P305 + P351 + P338 expand Show data source
Personal Protective Equipment
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter expand Show data source
Storage Temperature
2-8°C expand Show data source
Purity
≥98.0% (sum of enantiomers, GC) expand Show data source
98% expand Show data source
Grade
purum expand Show data source
Optical Purity
ee: 97% (GLC) expand Show data source
enantiomeric ratio: ≥98.25:1.75 (GC) expand Show data source
Certificate of Analysis
Download expand Show data source
Empirical Formula (Hill Notation)
C12H22O3 expand Show data source

DETAILS

DETAILS

MP Biomedicals MP Biomedicals Sigma Aldrich Sigma Aldrich
MP Biomedicals - 05213056 external link
MP Biomedicals Rare Chemical collection
Sigma Aldrich - M3000 external link
Packaging
1, 10 g in glass bottle
Sigma Aldrich - 63685 external link
Other Notes
Reagent for the resolution of amines, amino acids, alcohols and phenols1,2,3

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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