CAS 15761-39-4|Boc-L-Proline

Introduction：Basic information about CAS 15761-39-4|Boc-L-Proline, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. Boc-L-Proline BiologicalActivity
3. Chemical & Physical Properties
4. Safety Information
5. Customs
6. Articles2
7. Synonyms

Common Name	Boc-L-Proline
CAS Number	15761-39-4	Molecular Weight	215.25
Density	1.2±0.1 g/cm3	Boiling Point	337.2±35.0 °C at 760 mmHg
Molecular Formula	C₁₀H₁₇NO₄	Melting Point	133-136ºC
MSDS	USA	Flash Point	157.7±25.9 °C

Names

Name	BOC-L-Proline
Synonym	More Synonyms

Boc-L-Proline BiologicalActivity

Description	Boc-L-proline is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog	Research Areas >>OthersSignaling Pathways >>Others >>Others

Chemical & Physical Properties

Density	1.2±0.1 g/cm3
Boiling Point	337.2±35.0 °C at 760 mmHg
Melting Point	133-136ºC
Molecular Formula	C₁₀H₁₇NO₄
Molecular Weight	215.25
Flash Point	157.7±25.9 °C
Exact Mass	215.115753
PSA	66.84000
LogP	0.56
Vapour Pressure	0.0±1.6 mmHg at 25°C
Index of Refraction	1.503
InChIKey	ZQEBQGAAWMOMAI-ZETCQYMHSA-N
SMILES	CC(C)(C)OC(=O)N1CCCC1C(=O)O
Storage condition	2~8°C

Safety Information

Personal Protective Equipment	Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes	Xn
Risk Phrases	20/21/22-36/37/38
Safety Phrases	S24/25
RIDADR	NONH for all modes of transport
WGK Germany	3
HS Code	2933990090

Customs

HS Code	2933990090
Summary	2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles2

Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Nat. Chem. Biol. 5 , 45-52, (2009)

Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr...

Complexation-Driven Mutarotation in Poly(L-proline) Block Copolypeptides.

Biomacromolecules 16 , 3686-93, (2015)

Novel poly(L-lysine)-block-poly(L-proline) (PLL-b-PLP)-based materials with all PLP helical conformers, i.e., PLP II and the rare PLP I are here reported. Electrostatic supramolecular complexation of ...

Synonyms

1-(tert-butoxycarbonyl)-L-proline

Boc-L-Pro-OH

tert-Butyloxycarbonyl-L-proline

1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)-

N-(tert-Butyloxycarbonyl)-L-proline

MFCD00037324

1-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-proline

Boc-L-Proline

1,2-Pyrrolidinedicarboxylic acid, 1- (1,1-dimethylethyl) ester, (S)-

EINECS 239-848-3

N-(tert-Butoxycarbonyl)-L-proline

(S)-1-(tert-Butoxycarbonyl)pyrrolidine-2-carboxylic acid

(2S)-1-{[(2-Methyl-2-propanyl)oxy]carbonyl}-2-pyrrolidinecarboxylic acid

N-Boc-L-proline

1-tert-Butyloxycarbonyl-L-proline

Boc-Pro-OH

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