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462063

Sigma-Aldrich

(R)-(+)-3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde

95%

Synonym(s):

(+)-N-Boc-N,O-isopropylidene-D-serinal, tert-Butyl (R)-(+)-4-formyl-2,2-dimethyl-3-oxazolidinecarboxylate

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About This Item

Empirical Formula (Hill Notation):
C11H19NO4
CAS Number:
95715-87-0
Molecular Weight:
229.27
Beilstein:
3651554
MDL number:
MFCD00674064
UNSPSC Code:
12352005
PubChem Substance ID:
24869933
NACRES:
NA.22

Quality Level

100

Assay

95%

optical activity

[α]23/D +90°, c = 1 in chloroform

impurities

<6% methyl (R)-(+)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-oxazolidinecarboxylate (CAS 95715-87-0)

refractive index

n20/D 1.445 (lit.)

bp

67 °C/0.3 mmHg (lit.)

density

1.06 g/mL at 25 °C (lit.)

functional group

aldehyde
ether

SMILES string

[H]C(=O)[C@H]1COC(C)(C)N1C(=O)OC(C)(C)C

InChI

1S/C11H19NO4/c1-10(2,3)16-9(14)12-8(6-13)7-15-11(12,4)5/h6,8H,7H2,1-5H3/t8-/m0/s1

InChI key

PNJXYVJNOCLJLJ-QMMMGPOBSA-N

Related Categories

Application

Employed in the synthesis of fluorinated analogs of glutemic and glutamine.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

215.6 °F - closed cup

Flash Point(C)

102 °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 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

462063-1G:
462063-BULK:
462063-250MG:
462063-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCG9642
MKBK6884V
MKBG6657V
MKBF3481V
MKBF3481

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R Dave et al.
Amino acids, 24(3), 245-261 (2003-04-23)
Gamma-fluorinated analogues of glutamic acid and glutamine are compounds of biological interest. Syntheses of such compounds are extensively reviewed in this article. 4-fluoroglutamic acid was prepared as a mixture of racemic diastereomers by Michael reaction, inverse-Michael reaction or by electrophilic

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