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1233249-35-8

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1233249-35-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1233249-35-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,3,2,4 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1233249-35:
(9*1)+(8*2)+(7*3)+(6*3)+(5*2)+(4*4)+(3*9)+(2*3)+(1*5)=128
128 % 10 = 8
So 1233249-35-8 is a valid CAS Registry Number.

1233249-35-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Boc-4-aminophenylacetonitrile

1.2 Other means of identification

Product number -
Other names 4-tert-butoxycarbonylaminophenylacetonitrile

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:1233249-35-8 SDS

1233249-35-8Relevant articles and documents

OXADIAZOLES AS FUNGICIDES

-

Page/Page column 63-64, (2020/05/15)

The present invention relates to novel oxadiazoles of Formula (I) wherein, R1, L1, A1, A2, A3, A4, L2 and R2 are as defined in the detailed description. The present in

The Concise Synthesis of Unsymmetric Triarylacetonitriles via Pd-Catalyzed Sequential Arylation: A New Synthetic Approach to Tri- and Tetraarylmethanes

Nambo, Masakazu,Yar, Muhammad,Smith, Joel D.,Crudden, Cathleen M.

supporting information, p. 50 - 53 (2015/07/28)

The selective synthesis of multiarylated acetonitriles via sequential palladium-catalyzed arylations of chloroacetonitrile is reported. The three aryl groups are installed via a Pd-catalyzed Suzuki-Miyaura cross coupling reaction followed by back-to-back C-H arylations to afford triarylacetonitriles in three steps with no over-arylation at any step. The triarylacetonitrile products can be converted into highly functionalized species including tetraarylmethanes. This new strategy provides rapid access to a variety of unsymmetrical tri- and tetraarylmethane derivatives from simple, readily available starting materials. (Chemical Presented)

Isoquinoline derivatives as potent CRTH2 receptor antagonists: Synthesis and SAR

Nishikawa-Shimono, Rie,Sekiguchi, Yoshinori,Koami, Takeshi,Kawamura, Madoka,Wakasugi, Daisuke,Watanabe, Kazuhito,Wakahara, Shunichi,Matsumoto, Kayo,Takayama, Tetsuo

scheme or table, p. 3305 - 3310 (2012/06/18)

Synthesis and structure-activity relationship of a novel series of isoquinoline CRTH2 receptor antagonists are described. One of the most potent compounds, TASP0376377 (6m), showed not only potent binding affinity (IC 50 = 19 nM) but also excellent functional antagonist activity (IC50 = 13 nM). TASP0376377 was tested for its ability of a chemotaxis assay to show the effectiveness (IC50 = 23 nM), which was in good agreement with the CRTH2 antagonist potency. Furthermore, TASP0376377 showed sufficient selectivity for binding to CRTH2 over the DP1 prostanoid receptor (IC50 >1 μM) and COX-1 and COX-2 enzymes (IC 50 >10 μM).

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