ChemicalBook--->CAS DataBase List--->7531-52-4

7531-52-4

7531-52-4 Structure

7531-52-4 Structure
IdentificationMore
[Name]

L-Prolinamide
[CAS]

7531-52-4
[Synonyms]

2-PYRROLIDINECARBOXAMIDE, (2S)-
H-PRO-NH2
L-(-)-PROLINAMIDE
L-PROLINAMIDE
L-PROLINE AMIDE
L-PYRROLIDINE-2-CARBOXYLIC ACID AMIDE
PROLINAMIDE
PROLINE-NH2
(S)-PROLINAMIDE
(S)-PYRROLIDINE-2-CARBOXYLIC ACID AMIDE
(s)-(-)-pyrrolidin-2-carbonsaeureamid
(S)-pyrrolidine-2-carboxamide
L-PROLINAMIDE FREE BASE
Pro-Nh2
L-PROLINAMIDE 99.0%
H-Pro-NH2, free base
H-L-Pro-NH2
(S)-2-Pyrrolidinecarboxamide
L-Srolinamide, 98%
L-Pro-NH2
[EINECS(EC#)]

231-397-0
[Molecular Formula]

C5H10N2O
[MDL Number]

MFCD00005253
[Molecular Weight]

114.15
[MOL File]

7531-52-4.mol
Chemical PropertiesBack Directory
[Appearance]

Crystalline
[Melting point ]

95-97 °C (lit.)
[alpha ]

-106 º (c=2, EtOH)
[Boiling point ]

213.66°C (rough estimate)
[density ]

1.1008 (rough estimate)
[refractive index ]

1.4720 (estimate)
[storage temp. ]

-20°C
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Powder or Granules
[pka]

16.21±0.20(Predicted)
[color ]

White to straw
[Optical Rotation]

[α]20/D 106°, c = 2 in ethanol
[Water Solubility ]

Soluble in water and ethanol (50 mg/ml).
[Detection Methods]

GC
[BRN ]

80807
[Major Application]

peptide synthesis
[InChI]

1S/C5H10N2O/c6-5(8)4-2-1-3-7-4/h4,7H,1-3H2,(H2,6,8)/t4-/m0/s1
[InChIKey]

VLJNHYLEOZPXFW-BYPYZUCNSA-N
[SMILES]

NC(=O)[C@@H]1CCCN1
[CAS DataBase Reference]

7531-52-4(CAS DataBase Reference)
Questions And AnswerBack Directory
[Synthesis]

20% Pd(OH)₂/C (Pearlman catalyst, 80 mg) was added to a solution of the aminoamide adduct (175 mg, 0.8 mmol) in an EtOH/AcOH (1:1) (4 mL) mixture. The mixture was stirred at room temperature under H₂ (1 atm) for 14 hours. The mixture was degassed under an argon flow and filtered through diatomaceous earth. The collected solids were washed with EtOH (3 x 10 mL). The combined filtrate and washes were concentrated. The residue was neutralized with concentrated NH₄OH (2 mL). The mixture was placed in FC (eluent, MeOH/CH₂Cl₂/concentrated NH₄OH 50/50/1) to give L-prolylamide.


Figure 1 Synthetic route of L-Prolinamide

Figure 1 Synthetic route of L-Prolinamide

Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H317-H319
[Precautionary statements ]

P261-P271-P280
[Hazard Codes ]

Xn
[Risk Statements ]

R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
[WGK Germany ]

3
[F ]

10
[REACH Registrations]

Active
[HS Code ]

29339900
[Storage Class]

11 - Combustible Solids
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

L-Prolinamide(7531-52-4).msds
Hazard InformationBack Directory
[Chemical Properties]

Crystalline
[Uses]

Proline based organocatalyst.
[Definition]

ChEBI: The carboxamide derivative of L-proline.
[reaction suitability]

reaction type: solution phase peptide synthesis
Spectrum DetailBack Directory
[Spectrum Detail]

L-Prolinamide(7531-52-4)1HNMR
L-Prolinamide(7531-52-4)IR
L-Prolinamide(7531-52-4)Raman
L-Prolinamide(7531-52-4)FT-IR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

L-Prolinamide, 98%(7531-52-4)
[Alfa Aesar]

L-(-)-Prolinamide, 99%(7531-52-4)
[Sigma Aldrich]

7531-52-4(sigmaaldrich)
[TCI AMERICA]

L-Prolinamide,>97.0%(T)(7531-52-4)
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