Scholarly article on alpha-Chloro-p-fluorotoluene 352-11-4 from Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy p. 1605

DOI: 10.1016/0584-8539(75)80100-0

Source and publish data:

Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy p. 1605 (1975)

Update date:2022-08-28

Topics:

Authors:

Seth-Paul

Shino Shino

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/0584-8539(75)80100-0

Full text of DOI:10.1016/0584-8539(75)80100-0

Products guided by the article

Product name:alpha-Chloro-p-fluorotoluene

Cas No:352-11-4

R&D Labs maybe for 352-11-4

SHENZHEN PENGCHENG REDSTAR INDUSTRY CO.,LTD

Contact:+86-755-82412922

Address:Room 8066, East Block, Square City, Jiabin Road, Luohu District
NingBO Hong Xiang Biochem.Co.Ltd

website:http://www.hxbiochem.com

Contact:0574-66003444

Address:Ning Bo Bei Lun
Tianjin Te-An Chemtech Co., Ltd.(expird)

Contact:+86-22-65378638

Address:A5-8, No.80 Haiyun Street, TEDA
Chengdu NoVi Biotechnology Co., Ltd.(expird)

Contact:13551243286/028-81458053

Address:NO.168-1-224 JULONG ROAD WUHOU DISTRICT, CHENGDU CITY,SICHUAN PROVINCE
Weifang Adde Economic And Trade Co.,LTD.

Contact:86-536-8885548

Address:Room 1402,Wanda Plaza B Block,No.958,Yuanfei Road,Kuiwen District

Relevant to this article

Doi:10.1021/ja00515a023
(1979)
Poly(N-heterocyclic-carbene)s and their CO₂ adducts as recyclable polymer-supported organocatalysts for benzoin condensation and transesterification reactions

Doi:10.1021/ma1024285
(2011)
Synthesis of nanodiamond derivatives carrying amino functions and quantification by a modified kaiser test

Doi:10.3762/bjoc.10.288
(2014)
Proline-threonine dipeptide as an organocatalyst for the direct asymmetric aldol reaction

Doi:10.1016/j.tetasy.2009.06.018
(2009)
High-temperature sulfur removal from biomass-derived synthesis gas over bifunctional molybdenum catalysts

Doi:10.1002/cctc.201300185
(2013)
Transformation of N, N-Dimethylaniline N-Oxides into Diverse Tetrahydroquinoline Scaffolds via Formal Povarov Reactions

Doi:10.1021/acs.orglett.8b02318
(2018)

Article Doi

DOI: 10.1016/0584-8539(75)80100-0