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Merck
모든 사진(1)

주요 문서

모든 문서 보기

167037

Sigma-Aldrich

3-Methylsalicylic acid

96.0%

동의어(들):

2-Hydroxy-3-methylbenzoic acid, o-Cresotic acid

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모든 사진(1)

About This Item

Linear Formula:
CH3C6H3(OH)CO2H
CAS Number:
83-40-9
Molecular Weight:
152.15
Beilstein:
2086811
EC Number:
201-473-8
MDL number:
MFCD00002448
UNSPSC 코드:
12352100
PubChem Substance ID:
24850191
NACRES:
NA.22

분석

96.0%

mp

163-165 °C (lit.)

solubility

methanol: soluble 5%, clear to slightly hazy (colorlessto faint brown)

SMILES string

Cc1cccc(C(O)=O)c1O

InChI

1S/C8H8O3/c1-5-3-2-4-6(7(5)9)8(10)11/h2-4,9H,1H3,(H,10,11)

InChI key

WHSXTWFYRGOBGO-UHFFFAOYSA-N

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일반 설명

3-Methylsalicylic acid reacts with WOCl4 to yield tungsten(VI) oxo-salicylate complexes[1].

애플리케이션

3-Methylsalicylic acid was used in the synthesis of:
  • 8-methyl-2-thioxo-2,3-dihydro-4H-1,3-benzoxazin-4-one[2]
  • 7-hydroxy-8-methyl-2-thioxo-2,3-dihydro-4H-1,3-benzoxazin-4-one[2]
  • (R)-, (S)- and (RS)-hydroxymethylmexiletine[3]

픽토그램

CorrosionExclamation mark
GHS05,GHS07

신호어

Danger

유해 및 위험 성명서

H302,H315,H318,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
BCCB8094
BCBS4665V
BCBR1735V
BCBR0784V
BCBQ6247V

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문서 라이브러리 방문

이미 열람한 고객

Slide 1 of 1

1 of 1

Salicylic acid ACS reagent, ≥99.0%

Sigma-Aldrich

247588

Salicylic acid

Krithika Delhiraja et al.
Environmental monitoring and assessment, 192(7), 432-432 (2020-06-17)
Emerging contaminants (ECs) have become an increasing area of concern due to the likely impacts of these compounds on human health and the environment. Generally, products which are used for households and personal care activities contribute to major percentage of
Generalized Method for the Production of 1, 3-Benzoxazine, 1, 3-Benzothiazine, and Quinazoline Derivatives from 2-(Hydroxy, Thio, or Amino) Aromatic Acids Using Triphenylphosphine Thiocyanogen.
Pritchard KM, et al.
Synthetic Communications, 35(!2), 1601-1611 (2005)
Synthesis of (R)-, (S)-, and (RS)-hydroxymethylmexiletine, one of the major metabolites of mexiletine.
Cavalluzzi MM, et al.
Tetrahedron Asymmetry, 18(20), 2409-2417 (2007)
Alena A Antipova et al.
Genome biology, 9(3), R47-R47 (2008-03-04)
Here we describe a proof-of-concept experiment designed to explore the possibility of using gene expression-based high-throughput screening (GE-HTS) to find inhibitors of a signaling cascade, using platelet derived growth factor receptor (PDGFR) signaling as the example. The previously unrecognized ability
Thais Kroetz et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 18(5), 1171-1184 (2019-02-28)
In this article, new fluorescent lipophilic based benzazoles were synthesized from the reaction between photoactive formyl derivatives and aliphatic amines followed by NaBH4 reduction with good yields. The photophysics of the benzazoles was investigated experimentally and theoretically. These compounds present
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