Benzyl glycidyl ether

HCID 94247CAS 2930-05-4

기본 정보

표준 SMILES: c1ccc(COCC2CO2)cc1
InChIKey: QNYBOILAKBSWFG-UHFFFAOYSA-N
분자식: C10H12O2
평균 분자량: 164.2 g/mol
단동위원소 질량: 164.08372962

이름 및 식별자

우선 이름: Benzyl glycidyl ether
IUPAC: 2-(phenylmethoxymethyl)oxirane
영어명: Benzyl glycidyl ether
분자식: C10H12O2
분자량: 164.2

이름 및 동의어

Benzyl glycidyl etherRefChem:5667542930-05-42-((Benzyloxy)methyl)oxirane2-[(benzyloxy)methyl]oxirane89616-40-02-(Benzyloxymethyl)oxirane(Benzyloxymethyl)oxiraneOxirane, 2-[(phenylmethoxy)methyl]-Oxirane, [(phenylmethoxy)methyl]-2-(phenylmethoxymethyl)oxiranePropane, 1-(benzyloxy)-2,3-epoxy-

이름 더 보기

JX 011VITAS-BB TBB000194(Benzyloxy)methyl]benzolBenzyl glycidyl ether 99%Benzyl-2,3-epoxypropylether1-(benzyloxy)-2,3-epoxy-propan

(S)-(+)-Benzyl glycidyl ether1-(Benzyloxy)-2,3-epoxypropaneMFCD00068664Oxirane, ((phenylmethoxy)methyl)-[(Phenylmethoxy)methyl]oxirane (Benzyl Glycidyl Ether)benzyloxymethyloxiraneglycidyl benzyl ether1-Benzyloxy-2,3-epoxypropane

데이터베이스 식별자

CAS: 2930-05-4
PubChem CID: 94247
DTXSID: DTXSID001019317
EC Number: 920-007-0
Nikkaji: J64.257F

물성

구조 계산 물성

XLogP: 1.3
극성 표면적: 21.8 Å²
수소 결합 공여자 수: 0
수소 결합 수용자 수: 2
회전 가능 결합 수: 4
무거운 원자 수: 12
형식 전하: 0
복잡도: 130

물리화학적 성질

녹는점: 89.5 · 89.5-90.1 °C
끓는 점: 70 · 70-73 °C/11 mmHg (lit.)
밀도: 1.077 g/mL · 1.077 g/mL at 25 °C (lit.)
굴절률: 20 · n20/D 1.5170(lit.)
인화점: 230 °F · >230 °F
저장 조건: 2 · 2-8°C
물리적 상태: 투명한 액체
색상: 무색~연황색
InChIKey: QNYBOILAKBSWFG-UHFFFAOYSA-N

안전 및 규제

안전 데이터

wgk: 3
rtecs: TX2860000
HS 번호: 29329990
risk_code: 36/37/38
hazard_code: Xi
safety_code: 26-37/39

화학 및 산업

응용 분야 · 2건

용도[(Phenylmethoxy)methyl]oxirane, is a Glycidol (G615700) derivative. It is also shown that analougues of Phenyl Glycidyl Ether has in Vivo skin sensitizing potency, and is able to induce Nrf2-Dependent Luciferase Activity in the KeratinoSens.

일반 설명Benzyl glycidyl ether is a glycidyl derivative. Rac-/(R)-benzyl glycidyl ether participates in the synthesis of atactic and isotactic linear poly(benzyl 1,2-glycerol carbonate)s. Biocatalytic resolution of racemic benzyl glycidyl ether by Talaromyces flavus has been described. Resolution of benzyl glycidyl ether to (S)-benzyl glycidyl ether with 30% ee and (R)-3-benzyloxypropane-1,2-diol with 40% ee by whole Bacillus alcalophilus cells has been reported. It reacts with K-, K+(15-crown-5)2 to afford potassium glycidoxide and bibenzyl.