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16229-26-8

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16229-26-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16229-26-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,2 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16229-26:
(7*1)+(6*6)+(5*2)+(4*2)+(3*9)+(2*2)+(1*6)=98
98 % 10 = 8
So 16229-26-8 is a valid CAS Registry Number.

16229-26-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Hydrazinothieno[3,2-d]pyrimidine

1.2 Other means of identification

Product number -
Other names 4-Hydrazino-thieno<3,2-d>pyrimidin

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:16229-26-8 SDS

16229-26-8Relevant articles and documents

Synthesis of thienopyrimidine-pyrazolo[3,4-b]pyridine hybrids

Park, Jae Woo,Song, Yang-Heon

, p. 281 - 285 (2017)

New hybrid compounds, thienopyrimidinyl-1H-pyrazolo[3,4-b]pyridine derivatives, were efficiently synthesized by the three-component reaction of 3-phenyl-1-(thienopyrimidin-4-yl)-1H-pyrazol-5-amine, benzoylacetonitrile and an aromatic aldehyde in the prese

Facile synthesis of 2-phenylthieno[2,3-e][1,2,4]triazolo[1,5-c]pyrimidine derivatives as a new ring system

Song, Yang-Heon

scheme or table, p. 841 - 843 (2011/03/19)

A facile synthesis of 2-phenylthieno[2,3-e][1,2,4]triazolo[1,5-c] pyrimidine derivatives as a new ring system was presented. The compounds were prepared through a series of reaction starting with 3-aminothiophene-2- carbonitrile according to the modified

Discovery of novel small molecule cell type-specific enhancers of NF-κB nuclear translocation

Gong, Gangli,Xie, Yuli,Liu, Yidong,Rinderspacher, Alison,Deng, Shi-Xian,Feng, Yan,Zhu, Zhengxiang,Tang, Yufei,Wyler, Michael,Aulner, Nathalie,Toebben, Udo,Smith, Deborah H.,Branden, Lars,Chung, Caty,Schuerer, Stephan,Vidovic, Dusica,Landry, Donald W.

scheme or table, p. 1191 - 1194 (2009/08/07)

An IKKβ inhibitor reported to block NF-κB transcriptional activities in Jurkat T cells, was found to enhance NF-κB translocation in HUVEC cells. These studies suggested a noncanonical NF-κB signaling pathway independent of IKKβ in HUVEC cells.

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