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Merck
모든 사진(1)

주요 문서

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157147

Sigma-Aldrich

Valeroyl chloride

98%

동의어(들):

Pentanoic acid chloride, n-Butanecarbonyl chloride, n-Pentanoyl chloride, n-Valeryl chloride

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모든 사진(1)

About This Item

Linear Formula:
CH3(CH2)3COCl
CAS Number:
638-29-9
Molecular Weight:
120.58
Beilstein:
506293
EC Number:
211-330-1
MDL number:
MFCD00000757
UNSPSC 코드:
12352100
PubChem Substance ID:
24849658
NACRES:
NA.22

Quality Level

100

분석

98%

양식

liquid

refractive index

n20/D 1.42 (lit.)

bp

125-127 °C (lit.)

density

1.016 g/mL at 25 °C (lit.)

작용기

acyl chloride

SMILES string

CCCCC(Cl)=O

InChI

1S/C5H9ClO/c1-2-3-4-5(6)7/h2-4H2,1H3

InChI key

XGISHOFUAFNYQF-UHFFFAOYSA-N

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관련 카테고리

애플리케이션

Valeroyl chloride was used in the enantioselective synthesis of propylisopropyl acetamide (PID), an amide analog of the major antiepileptic drug valproic acid. It was also used in the synthesis of (4R, 5S-4-methyl-3-(1-oxopentyl)-5-phenyl-oxazolidinone.

픽토그램

FlameSkull and crossbonesCorrosion
GHS02,GHS06,GHS05

신호어

Danger

유해 및 위험 성명서

H226,H290,H314,H331,H412

Hazard Classifications

Acute Tox. 3 Inhalation - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 3 - Met. Corr. 1 - Skin Corr. 1A

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point (°F)

89.6 °F - closed cup

Flash Point (°C)

32 °C - closed cup

개인 보호 장비

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
BCCH5421
BCCH2061
BCCG1354
BCCB2843
BCBV1309

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특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

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문서 라이브러리 방문

R S Hauck et al.
Pharmaceutical research, 9(7), 850-855 (1992-07-01)
The teratogenic activities of R(+)- and S(-)-2-n-propyl-4-pentynoic acid (R and S-4-yn-VPA), the enantiomers of the highly teratogenic valproic acid (VPA) analogues (+/-)-4-yn-VPA, were investigated in mice. The enantiomers were prepared via asymmetric synthesis, each in three steps employing the chiral
O Spiegelstein et al.
Chirality, 11(8), 645-650 (1999-09-01)
Propylisopropyl acetamide (PID), an amide analogue of the major antiepileptic drug valproic acid (VPA), possesses favorable anticonvulsant and CNS properties. PID contains one chiral carbon atom and therefore exists in two enantiomeric forms. The purpose of this work was to
Janclei P Coutinho et al.
Talanta, 134, 256-263 (2015-01-27)
In this work a multivariate statistical tool (Derringer and Suich optimization) was proposed for the separation of seventeen capsinoids (natural and synthetic) using the UHPLC-DAD chromatography. Capsinoids were analyzed at 280 nm. The variables optimized were the mobile phase (water

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