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331317

Sigma-Aldrich

5-Bromovaleryl chloride

97%

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5 G
PLN 248.00
25 G
PLN 522.00

PLN 248.00

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5 G
PLN 248.00
25 G
PLN 522.00

About This Item

Linear Formula:
Br(CH2)4COCl
CAS Number:
4509-90-4
Molecular Weight:
199.47
MDL number:
MFCD00013660
UNSPSC Code:
12352100
PubChem Substance ID:
24859951
NACRES:
NA.22

PLN 248.00

Please contact Customer Service for Availability
Request a Bulk Order

Assay

97%

form

liquid

refractive index

n20/D 1.492 (lit.)

bp

116-118 °C/33 mmHg (lit.)

density

1.49 g/mL at 25 °C (lit.)

functional group

acyl chloride
bromo

SMILES string

ClC(=O)CCCCBr

InChI

1S/C5H8BrClO/c6-4-2-1-3-5(7)8/h1-4H2

InChI key

OKRUMSWHDWKGHA-UHFFFAOYSA-N

Application

5-Bromovaleryl chloride was used in the preparation of aromatic azides[1] and organic gelators.[2]

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H314,H335

Hazard Classifications

Eye Irrit. 2 - Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

224.6 °F - closed cup

Flash Point(C)

107 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000250299
0000250300
0000225458
0000250300
0000250299

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The role of the neutral and cationic gelators from (1S, 2S)-(-)-diphenylethylenediamine for the preparation of silica nano tubes.
Hyun MH, et al.
Bull. Korean Chem. Soc., 30(7), 1641-1643 (2009)
Rajavel Srinivasan et al.
Organic letters, 8(4), 713-716 (2006-02-14)
[reaction: see text] We have successfully designed and synthesized a small library of protein tyrosine phosphatase (PTP) inhibitors, in which the so-called "click chemistry" or Cu(I)-catalyzed 1,3-dipolar alkyne-azide coupling reaction was carried out for rapid assembly of 66 different bidentate
Duy Khuong Mai et al.
Molecules (Basel, Switzerland), 25(15) (2020-07-29)
The synthesis of three water-soluble lactose-modified 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY)-based photosensitizers with tumor-targeting capabilities is reported, including an investigation into their photodynamic therapeutic activity on three distinct cancer cell lines (human hepatoma Huh7, cervical cancer HeLa, and breast cancer MCF-7 cell lines).

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