物质信息

ID:715185

名称和标识
IUPAC传统名
triphenylmethyl chloride
IUPAC标准名
(chlorodiphenylmethyl)benzene
别名
Trityl chlorideTriphenylmethyl chloride三苯基氯甲烷Chlorotriphenylmethane
数据登录号
CAS号
Beilstein号
化合物性质
安全信息
GHS危险品标识
GHS09
对水环境的危害
急性危害,类别1
慢性危害,类别1,2
GHS05
腐蚀金属,类别1
腐蚀皮肤,类别1A,1B,1C
严重眼损伤,类别1
欧盟危险性物质标志
环境危害性 环境危害性 (N)
腐蚀性 腐蚀性 (C)
危险公开号
34-50/53
联合国危险货物等级
8
RTECS编号
PA6450000
联合国危险货物编号
UN3261
联合国危险货物包装类别(PG)
II
GHS警示性声明
P280-P273-P305+P351+P338-P309-P310
TSCA收录
GHS危险声明
H314-H318-H400-H410
安全公开号
26-36/37/39-45-60-61
保存注意事项
Moisture Sensitive
理化性质
沸点
230-235°C/20mm
熔点
110-114°C
产品相关信息
纯度
98%
描述信息
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分子图谱
暂无数据
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参考文献
• Progressively more acid-labile protecting groups contain one, two or three p-methoxy-groups: 4-Methoxytrityl chloride, A10545, 4,4'-Dimethoxytrityl chloride, A11626, and 4,4',4''-Trimethoxytrityl chloride, L00629, respectively.
• Reagent for protection of N, S and particularly O functions as trityl (Trt) derivatives, stable to a wide range of conditions, but readily cleaved by mild acid.
• For an improved method for O-tritylation in triethylamine in the presence of catalytic amounts of DMAP, see: Tetrahedron Lett., 95 (1979).
• For a one-pot procedure for the high yield, racemization-free N-tritylation of amino acids, by means of prior in situ O-silylation, see: J. Org. Chem., 47, 1324 (1982). N-Trt- derivatives of amino acids have also been converted to Leuchs' anhydrides by treatment with phosgene or triphosgene, and the products coupled with amino acid esters to give dipeptides in good yields without racemization: J. Org. Chem., 64, 2532 (1999). See also 9-Bromo-9-phenylfluorene, L14225.