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Safety Information

483761

Sigma-Aldrich

Boc-L-prolinal

97%

Synonym(s):

(S)-N-Boc-pyrrolidine-2-carboxaldehyde, N-(tert-Butoxycarbonyl)-L-prolinal

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About This Item

Empirical Formula (Hill Notation):
C10H17NO3
CAS Number:
69610-41-9
Molecular Weight:
199.25
MDL number:
MFCD00274186
UNSPSC Code:
12352209
PubChem Substance ID:
24871916
NACRES:
NA.22

Assay

97%

optical activity

[α]20/D −101°, c = 0.66 in chloroform

reaction suitability

reaction type: Boc solid-phase peptide synthesis

refractive index

n20/D 1.462 (lit.)

bp

211 °C (lit.)

density

1.063 g/mL at 25 °C (lit.)

application(s)

peptide synthesis

storage temp.

−20°C

SMILES string

[H]C(=O)[C@@H]1CCCN1C(=O)OC(C)(C)C

InChI

1S/C10H17NO3/c1-10(2,3)14-9(13)11-6-4-5-8(11)7-12/h7-8H,4-6H2,1-3H3/t8-/m0/s1

InChI key

YDBPZCVWPFMBDH-QMMMGPOBSA-N

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Application

Key building block for norsecurinine-type alkaloids and isaindigotidione carboskeleton.

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

135.0 °F - closed cup

Flash Point(C)

57.2 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

483761-VAR:
483761-1G:
483761-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
MKBZ8629V
MKBW4085V
MKBT2654V
MKBG9750V
MKBF1181V

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Tetrahedron Letters, 45, 2985-2985 (2004)
Ramon Alibés et al.
Organic letters, 6(11), 1813-1816 (2004-05-21)
The syntheses of securinine and (-)-allonorsecurinine have been achieved starting from easily available alpha-amino acid derivatives and using as key steps a RCM and a Heck reaction for the formation of rings D and C, respectively. [reaction: see text]

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