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306800

Sigma-Aldrich

(R)-(+)-2-Chloropropionic acid

99%

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About This Item

Linear Formula:
CH3CH(Cl)CO2H
CAS Number:
Molecular Weight:
108.52
Beilstein:
1720258
MDL number:
UNSPSC Code:
12352101
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

liquid

optical activity

[α]20/D +14°, neat

refractive index

n20/D 1.4345 (lit.)

bp

185-188 °C (lit.)

density

1.258 g/mL at 20 °C (lit.)

SMILES string

C[C@@H](Cl)C(O)=O

InChI

1S/C3H5ClO2/c1-2(4)3(5)6/h2H,1H3,(H,5,6)/t2-/m1/s1

InChI key

GAWAYYRQGQZKCR-UWTATZPHSA-N

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Application

(R)-(+)-2-Chloropropionic acid can be used as a starting material in the synthesis of:       
  • Thiolactic acid, a key intermediate, which is used for the preparation of 2(R),5(S)-oxathiolanones by reacting with pivalaldehyde.       
  • (R)-2-chloropropionyl chloride, a key intermediate, which is utilized in the synthesis of (R)-4,5-dihydro-5-methylpyridazin-3(2H)-one derivative with pyrazolopyridine ring as a potential phosphodiesterase inhibitor.       
  • 2-Chloropropionamide derivatives as protein disulfide isomerase (PID) inhibitors.

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

213.8 °F - closed cup

Flash Point(C)

101 °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

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

306800-1G:4548174002773
306800-VAR:
306800-BULK:


Certificates of Analysis (COA)

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Cedric L Hugelshofer et al.
The Journal of organic chemistry, 84(21), 14069-14091 (2019-09-20)
We provide a full account of our synthetic studies targeting the hexacyclic calyciphylline B-type alkaloids, a subfamily of the Daphniphyllum natural products. Following an initial set of synthetic strategies focused on constructing the piperidine core of the calyciphylline B-type framework

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