93000
Trityl chloride
purum, ≥97.0% (HPLC), ≥97.0% (AT)
동의어(들):
Chlorotriphenylmethane, Triphenylchloromethane, Triphenylmethyl chloride
로그인조직 및 계약 가격 보기
모든 사진(3)
About This Item
Linear Formula:
(C6H5)3CCl
CAS Number:
Molecular Weight:
278.78
Beilstein:
397363
EC Number:
MDL number:
UNSPSC 코드:
12352101
PubChem Substance ID:
NACRES:
NA.22
추천 제품
grade
purum
Quality Level
분석
≥97.0% (AT)
≥97.0% (HPLC)
양식
powder
무기 잔류물
≤0.2% (as SO4)
bp
230-235 °C/20 mmHg (lit.)
mp
109-112 °C (lit.)
109-113 °C
solubility
chloroform: 0.1 g/mL, clear
작용기
chloro
phenyl
SMILES string
ClC(c1ccccc1)(c2ccccc2)c3ccccc3
InChI
1S/C19H15Cl/c20-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
InChI key
JBWKIWSBJXDJDT-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
- Organic Synthesis: Research on the synthesis of 1, 2, 4-triazine derivatives, exploring the condensation reactions of trityl chloride with various compounds (Majid et al., 2020).
기타 정보
Reagent for tritylations;; Efficient method of tritylation of sensitive compounds and their subsequent detritylation
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
가장 최신 버전 중 하나를 선택하세요:
이미 열람한 고객
S J Harding et al.
Journal of peptide science : an official publication of the European Peptide Society, 5(8), 368-373 (1999-10-03)
A rational attempt to prepare FmocHis(piTrt)OH regiospecifically gave in fact the well-known tau-trityl isomer, and experiments with model systems indicate that the prospects for access to pi-trityl histidine derivatives, which would be of great value for the racemization-free synthesis of
K. Barlos et al.
The Journal of Organic Chemistry, 47, 1324-1324 (1982)
Vijayavitthal T Mathad et al.
Natural product research, 20(12), 1053-1058 (2006-11-28)
Jones oxidation of Andrographolide (1), gave mixture of three products (3-dehydroandrographolide (5), 3,19-bis dehydroandrographolide (6) and 19-dehydroandrographolide (7). Tritylation of andrographolide at C19-OH resulted to products 8 and diene 9, which can be converted to its acetate 10 and oxidation
Ryuichi Hasegawa et al.
Congenital anomalies, 45(4), 137-145 (2005-12-20)
To elucidate the comparative susceptibility of newborn rats to chemicals, newborn and young animals were administered six industrial chemicals by gavage from postnatal days (PND) 4 to 21, and for 28 days starting at 5-6 weeks of age respectively, under
R Hasegawa et al.
Regulatory toxicology and pharmacology : RTP, 47(3), 296-307 (2006-12-13)
We comprehensively re-analyzed the toxicity data for 18 industrial chemicals from repeated oral exposures in newborn and young rats, which were previously published. Two new toxicity endpoints specific to this comparative analysis were identified, the first, the presumed no observed
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