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102240-27-7

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102240-27-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102240-27-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,2,4 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 102240-27:
(8*1)+(7*0)+(6*2)+(5*2)+(4*4)+(3*0)+(2*2)+(1*7)=57
57 % 10 = 7
So 102240-27-7 is a valid CAS Registry Number.

102240-27-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,5-trimethoxy-benzoic acid-(3,4-dimethoxy-phenethylamide)

1.2 Other means of identification

Product number -
Other names N-(3.4-Dimethoxyphenethyl)-3.4.5-trimethoxybenzamid

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:102240-27-7 SDS

102240-27-7Relevant articles and documents

Josiphos-Type Binaphane Ligands for Iridium-Catalyzed Enantioselective Hydrogenation of 1-Aryl-Substituted Dihydroisoquinolines

Nie, Huifang,Zhu, Yupu,Hu, Xiaomu,Wei, Zhao,Yao, Lin,Zhou, Gang,Wang, Pingan,Jiang, Ru,Zhang, Shengyong

supporting information, p. 8641 - 8645 (2019/10/17)

Convenient synthesis and useful application of a series of Josiphos-type binaphane ligands were described. The iridium complexes of these chiral diphosphines displayed excellent enantioselectivity and good reactivity in the asymmetric hydrogenation of challenging 1-aryl-substituted dihydroisoquinoline substrates (full conversions, up to >99% ee, 4000 TON). The use of 40% HBr (aqueous solution) as an additive dramatically improved the asymmetric induction of these catalysts. This transformation provided a highly efficient and enantioselective access to chiral 1-aryl-substituted tetrahydroisoquinolines, which were of great importance and common in natural products and biologically active molecules.

Potential resperine analogues. Part I. Derivatives of tryptamine.

KARIM,LINNELL,SHARP

, p. 74 - 81 (2007/10/05)

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