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38378-77-7

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38378-77-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38378-77-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,7 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 38378-77:
(7*3)+(6*8)+(5*3)+(4*7)+(3*8)+(2*7)+(1*7)=157
157 % 10 = 7
So 38378-77-7 is a valid CAS Registry Number.

38378-77-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name anthracene-1,8-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names Anthracen-1,8-dicarbonsaeure

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:38378-77-7 SDS

38378-77-7Relevant articles and documents

Solid-state esterification via ionic-to-covalent bond transformation in ionic molecular crystals consisting of disubstituted anthracene anion-cation combinations

Suzuki, Masato,Fujii, Takahiro,Naito, Yoko,Yamoto, Kazuhisa,Matsuoka, Shin-Ichi,Takagi, Koji,Sugiyama, Haruki,Uekusa, Hidehiro

, p. 343 - 348 (2018/03/21)

Thermal solid-state reactions involving ionic-to-covalent bond transformation were achieved in the ionic molecular crystals of 1,8-bis[(pyridin-1-ium-1-yl)methyl]anthracene anthracene-1,8-dicarboxylate to produce the cyclic diester. The crystal structure given by X-ray diffraction analysis showed that the electrostatic interaction between the benzyl pyridinium cation and the carboxylate anion successfully works to locate these reaction sites close to each other and that there are channels for crystalline solvents and the liberated pyridine to escape. There by, the cyclic diester was selectively formed by the crystal-to-crystal reaction, which was proven by powder XRD profiles and optical microscopic and SEM images of the crystals before and after the reaction. This is the first thermal crystal-to-crystal condensation reaction. Another ionic molecular crystal of 1,8-bis[(pyridin-1-ium-1-yl)methyl]anthracene anthraquinone-1,8-dicarboxylate was also studied. There in, the corresponding cyclic diester was also obtained, but the crystals were transformed to amorphous solid by the reaction.

A host-guest system based on collagen-like triple-helix hybridization

Delsuc,Uchinomiya,Ojida,Hamachi

supporting information, p. 6856 - 6859 (2017/07/10)

A strategy inspired by tweezer receptors has been employed to develop a new host-guest system. The hybridization into a collagen-like triple helix is the driving force for the recognition that occurs with high affinity and selectivity. Several systems have been screened to find the best host-guest pair and this strategy may be implemented for tag fused protein recognition.

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