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416436

二苄基 N,N-二异丙基亚磷酰胺

Name: 二苄基 <I>N</I>,<I>N</I>-二异丙基亚磷酰胺
Brand: ALDRICH

technical grade, 90%

别名:

N,N-二异丙基二苄基磷酰胺, [双(苄氧基)膦基]双(丙烷-2-基)胺, 二苄基N,N-二异丙基磷酰胺, 二苄基二异丙基磷酰胺, 双(苄氧基)(二异丙基氨基)膦

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关于此项目

线性分子式:

[(CH₃)₂CH]₂NP(OCH₂C₆H₅)₂

化学文摘社编号:

108549-23-1

分子量:

345.42

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24866075

MDL number:

MFCD00191988

Beilstein/REAXYS Number:

3616864

Assay:

90%

Form:

liquid

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属性

grade

technical grade

Quality Level

200

assay

90%

form

liquid

refractive index

n20/D 1.535 (lit.)

bp

130 °C/0.55 mmHg (lit.)

solubility

THF: soluble(lit.), acetonitrile: soluble(lit.), cold water: insoluble(lit.), dichloromethane: soluble(lit.)

density

1.028 g/mL at 25 °C (lit.)

functional group

amine, phenyl

storage temp.

2-8°C

SMILES string

CC(C)N(C(C)C)P(OCc1ccccc1)OCc2ccccc2

InChI

1S/C20H28NO2P/c1-17(2)21(18(3)4)24(22-15-19-11-7-5-8-12-19)23-16-20-13-9-6-10-14-20/h5-14,17-18H,15-16H2,1-4H3

InChI key

ANPWLBTUUNFQIO-UHFFFAOYSA-N

说明

Application

N,N-二异丙基亚磷酰胺基二苄基酯可用于制备磷酸肽。它可用于合成GDP（鸟苷二磷酸）类似物SML-8-73-1。

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

156.2 °F - closed cup

flash_point_c

69 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Solid-phase synthesis of a range of O-phosphorylated peptides by post-assembly phosphitylation and oxidation.

D M Andrews et al.

International journal of peptide and protein research, 38(5), 469-475 (1991-11-01)

A completely general method for the O-phosphorylation of peptides of any given composition using solid-phase methodology is described. Peptides were assembled using Fmoc amino acid active esters, with base used for Fmoc deprotection. Unprotected amino acid side chain hydroxyl groups

Therapeutic targeting of oncogenic K-Ras by a covalent catalytic site inhibitor.

Sang Min Lim et al.

Angewandte Chemie (International ed. in English), 53(1), 199-204 (2013-11-22)

We report the synthesis of a GDP analogue, SML-8-73-1, and a prodrug derivative, SML-10-70-1, which are selective, direct-acting covalent inhibitors of the K-Ras G12C mutant relative to wild-type Ras. Biochemical and biophysical measurements suggest that modification of K-Ras with SML-8-73-1

A new reaction for the direct conversion of 4-azido-4-deoxy-D-galactoside into a 4-deoxy-D-erythro-hexos-3-ulose.

Jie Xue et al.

Organic letters, 6(9), 1365-1368 (2004-04-23)

[reaction: see text] A new one-step reaction has been developed for converting 4-azido-4-deoxy-d-galactoside into 4-deoxy-d-erythro-hexos-3-ulose by phosphoramidites and tetrazole. It is proposed that the new reaction proceeds via an intramolecular Staudinger reaction of the phosphite intermediate and a tetrazole-catalyzed elimination

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全球贸易项目编号

货号	GTIN
416436-5ML	04061837657184
416436-25ML	04061837657177