(R)-(-)-3-Carbamoymethyl-5-methylhexanoicacid CAS 181289-33-8

• Identification
• Properties
• Safety Data
• Specifications & Other Information
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Identification

CAS Number

181289-33-8

Name

(R)-(-)-3-Carbamoymethyl-5-methylhexanoicacid CAS 181289-33-8

Synonyms

(3R)-3-(2-Amino-2-oxoethyl)-5-methylhexanoic acid
[IUPAC name – generated by ACD/Name]
(3R)-3-(2-Amino-2-oxoethyl)-5-methylhexansäure
[German]
[IUPAC name – generated by ACD/Name]
(R)-(−)-3-(Carbamoylmethyl)-5-methylhexanoic acid
(R)-3-(2-Amino-2-oxoethyl)-5-methylhexanoic acid
11747721
[Beilstein]
181289-33-8
[RN]
185815-61-6
[RN]
Acide (3R)-3-(2-amino-2-oxoéthyl)-5-méthylhexanoïque
[French]
[IUPAC name – generated by ACD/Name]
Hexanoic acid, 3-(2-amino-2-oxoethyl)-5-methyl-, (3R)-
[Index name – generated by ACD/Name]
ZV1Y1VQ1Y1&1 &&R For
[WLN]

SMILES

CC(C)CC@HCC(=O)O

StdInChI

InChI=1S/C9H17NO3/c1-6(2)3-7(4-8(10)11)5-9(12)13/h6-7H,3-5H2,1-2H3,(H2,10,11)(H,12,13)/t7-/m1/s1

StdInChIKey

NPDKTSLVWGFPQG-SSDOTTSWSA-N

Molecular Formula

C9H17NO3

Molecular Weight

187.239

Beilstein Registry Number

11747721

MDL Number

MFCD09028111

Properties

Appearance

White powder

Safety Data

Symbol

GHS07

Signal Word

Warning

Hazard statements

H315

Precautionary Statements

P264 – P280 – P302 + P352 – P332 + P313 – P362 + P364

RIDADR 

NONH for all modes of transport

WGK Germany

3

Specifications and Other Information of Our (R)-(-)-3-Carbamoymethyl-5-methylhexanoicacid CAS 181289-33-8

Identification Methods

HNMR, IR, HPLC

Chiral Purity RIsomer

99% min

Any individual impurity

99% min

Chromatographic Purity

≤0.5%

Total Impurities

≤1.0%

Assay (By titrimetric)

98.5% ~102.0%

Water Content by KFR

≤1.0%

Shelf Life

1 year

Storage

Store in a cool place and protect from light

Known Application

(R)-(-)-3-(Carbamoylmethyl)-5-methylhexanoic acid is an intermediate in chiral organic synthesis; its primary application is to serve as a molecular scaffold in the synthesis of chiral pharmaceutical molecules and biologically active compounds. Under appropriate conditions, (R)-(-)-3-(carbamoylmethyl)-5-methylhexanoic acid can undergo an intramolecular cyclization reaction (lactamization) to yield chiral (R)-3-isobutylglutarimide.

Links

This product is developed by our R&D company Caming Pharmaceutical Ltd (https://www.caming.com/).

This product is developed by our R&D company Watson International Ltd (https://www.watson-int.com/).