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Merck

13030

Sigma-Aldrich

2-(苯甲酰氧甲基)苯甲酸

≥98.0% (T)

别名:

2-(羟甲基)苯甲酸苯甲酸酯

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About This Item

经验公式(希尔记法):
C15H12O4
CAS号:
分子量:
256.25
Beilstein:
2131052
EC號碼:
MDL號碼:
分類程式碼代碼:
12352108
PubChem物質ID:
NACRES:
NA.22

化驗

≥98.0% (T)

mp

126-129 °C

應用

peptide synthesis

SMILES 字串

OC(=O)c1ccccc1COC(=O)c2ccccc2

InChI

1S/C15H12O4/c16-14(17)13-9-5-4-8-12(13)10-19-15(18)11-6-2-1-3-7-11/h1-9H,10H2,(H,16,17)

InChI 密鑰

QDENBWUYSUBCID-UHFFFAOYSA-N

應用

2-(Benzoyloxymethyl)benzoic acid can be used to synthesize:
  • 2-(Benzoyloxymethyl)benzoyl chloride (BMBC) by reacting with oxalyl chloride. BMBC intermediate is utilized for the preparation of dimethyl 2-(benzoyloxymethyl)benzoylphosphonate by treating with trimethyl phosphite.
  • 2-Benzoyloxymethylbenzoic acid 4-nitrophenyl ester by reaction with 4-nitrophenol via 2-benzoyloxymethylbenzoyl chloride formation.
  • 2-[2-(Benzoyloxymethyl)benzamido]acetamide by treating with glycinamide and followed by addition of PCl3.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Cyclisation reactions of 2-substituted benzoylphosphonates with trialkyl phosphites via nucleophilic attack on a carbonyl-containing ortho substituent
Cheong Y-K, et al.
Tetrahedron, 64(10), 2329-2338 (2008)
2-Acyloxymethylbenzoic acids. Novel amine protective functions providing amides with the lability of esters
Cain BF
The Journal of Organic Chemistry, 41(11), 2029-2031 (1976)

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