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Phosphonic acid, [1,2,3,4-tetrahydro-2-(2-methoxyphenyl)-1-isoquinolinyl]-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87992-96-9

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87992-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87992-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,9,9 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 87992-96:
(7*8)+(6*7)+(5*9)+(4*9)+(3*2)+(2*9)+(1*6)=209
209 % 10 = 9
So 87992-96-9 is a valid CAS Registry Number.

87992-96-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl (2-(2-methoxyphenyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)phosphonate

1.2 Other means of identification

Product number -
Other names diethyl(2-(2-methoxyphenyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)phosphonate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:87992-96-9 SDS

87992-96-9Relevant academic research and scientific papers

A Porous and Stable Porphyrin Metal-Organic Framework as an Efficient Catalyst towards Visible-Light-Mediated Aerobic Cross-Dehydrogenative-Coupling Reactions

Liu, Jiewei,Zhang, Kun,Chen, Zhiyao,Wei, Zhang-Wen,Zhang, Li

supporting information, p. 1118 - 1124 (2020/03/10)

Porphyrin metal-organic frameworks (PMOFs) are emerging as heterogeneous photocatalysts owing to the well-designed frameworks incorporated with powerful light-harvesting porphyrin chromophores. The porous and stable framework Ir?PCN-224 (which is also den

Electrochemical Cross-Dehydrogenative Coupling of N-Aryl-tetrahydroisoquinolines with Phosphites and Indole

Xie, Wenxia,Liu, Nian,Gong, Bowen,Ning, Shulin,Che, Xin,Cui, Lili,Xiang, Jinbao

, p. 2498 - 2501 (2019/04/01)

A metal- and reagent-free, electrochemical cross-dehydrogenative coupling reaction of N-aryl-tetrahydroisoquinolines with phosphites and indole is developed. This method provides an environmentally benign and simple approach for the construction of C–P an

Iron-catalyzed aerobic oxidative phosphonation of N-aryl tetrahydroisoquinolines

Cai, Junjie,Liu, Yingle,Jiang, Yan,Yang, Yi

supporting information, p. 1068 - 1073 (2017/09/08)

We report herein a novel and efficientmethod for iron-catalyzed aerobic oxidative phosphonation of N-aryl tetrahydroisoquinolines for the synthesis of biologically interesting α-aminophosphonates. This new C–P bond formation reaction features the employme

A preparation method of the compound α - phosphoramidate

-

Paragraph 0060; 0061; 0062, (2017/11/01)

The invention discloses a preparation method of an alpha-phosphoramidate compound. The preparation method comprises the following steps: by taking low-molecular alcohol as a reaction solvent and taking N-phenyl-1,2,3,4-tetrahydroisoquinoline and dialkyl p

Thiourea-Catalyzed Cross-Dehydrogenative Coupling of C(sp3)–H with Diethyl Phosphite

Gu, Kai,Zhang, Zhiguo,Bao, Zongbi,Xing, Huabin,Yang, Qiwei,Ren, Qilong

supporting information, p. 3939 - 3942 (2016/08/24)

The efficient thiourea-catalyzed cross-dehydrogenative coupling of C(sp3)–H with diethyl phosphite by using tert-butyl peroxide as a terminal oxidant was explored. This protocol further expands the application scope of H-bond donors and also pr

A scalable, efficient gold-catalyzed oxidative phosphonation of sp 3 C-H bonds using air as sustainable oxidant

Xie, Jin,Li, Huamin,Xue, Qicai,Cheng, Yixiang,Zhu, Chengjian

supporting information; experimental part, p. 1646 - 1650 (2012/07/28)

A scalable, efficient gold-catalyzed oxidative phosphonation of sp 3 C-H bonds with various diarylphosphine oxides and dialkyl phosphites has been developed by using air as a sustainable oxidant under mild reaction conditions. It provides an ea

Eosin y catalyzed visible light oxidative C-C and C-P bond formation

Hari, Durga Prasad,Koenig, Burkhard

, p. 3852 - 3855 (2011/09/19)

Eosin Y catalyzes efficiently the visible light mediated coupling of sp3 C-H bonds adjacent to the nitrogen atom in tetrahydroisoquinoline derivatives in the absence of an external oxidant. Nitroalkanes, dialkyl malonates, malononitrile, and di

α-Substituted Phosphonates. 43. Synthesis and Reactivity of 1,2,3,4-Tetrahydroisoquinolin-1-phosphonates

Gross, H.,Ozegowski, S.

, p. 437 - 445 (2007/10/02)

N-Alkyl- and N-arylsubstituted 1,2,3,4-tetrahydroisochinolin-1-phosphonates 1 have been synthesized from the corresponding 3,4-dihydroisochinoliniumbromides 7 and triethylphosphite.The N-unsubstituted 1,2,3,4-tetrahydroisochinolin-1-phosphonate 10 is available starting from the 1,2,3,4-tetrahydroisochinolin-1-phosphonic acid by esterification with triethylformate and splitting off the formyl group of the primarily formed N-formyl derivative 14. - N-Quarternated tetrahydroisochinolines 19 and the 1-phosphorylated derivatives 17, respectively react with triethylphosphite in an unexpected way by dealkylation and not by splitting off the isochinolinring. - By Horner-synthesis with 1 the 1-aralkylidene-isochinolines 23 are available in moderate yields.

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