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1,3,4-Thiadiazole

Product Name
1,3,4-Thiadiazole
CAS No.
289-06-5
Chemical Name
1,3,4-Thiadiazole
Synonyms
1,3,4-thiadiazole;Ceftezole Impurity 15;Ceftezole Impurity 12
CBNumber
CB9842733
Molecular Formula
C2H2N2S
Formula Weight
86.12
MOL File
289-06-5.mol
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1,3,4-Thiadiazole Property

Melting point:
42.5°C
Boiling point:
204°C
Density 
1.299 (estimate)
refractive index 
1.5300 (estimate)
form 
solid
pka
-0.33±0.10(Predicted)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H312Harmful in contact with skin

H315Causes skin irritation

H319Causes serious eye irritation

H332Harmful if inhaled

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P312Call a POISON CENTER or doctor/physician if you feel unwell.

P321Specific treatment (see … on this label).

P322Specific measures (see …on this label).

P330Rinse mouth.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P362Take off contaminated clothing and wash before reuse.

P363Wash contaminated clothing before reuse.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
CHM0985325
Product name
1,3,4-THIADIAZOLE
Purity
95.00%
Packaging
5MG
Price
$502.49
Updated
2021/12/16
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1,3,4-Thiadiazole Chemical Properties,Usage,Production

Description

1,3,4-Thiadiazole is a five-membered, aromatic, weakly basic, planer, electron-deficient, conjugated heterocyclic ring system comprised of two carbon atoms, one sulfur atom, and two pyridine-like nitrogen atoms present at the 3- and 4-positions of the ring. The dipole moment (3.25 D) for 1,3,4-thiadiazole suggests that it is a polar symmetric molecule with pseudo-aromatic character. The carbon atoms at the 2- and 5-positions are electron deficient because of the inductive effect of nitrogen and sulfur and thus they are inert toward electrophilic substitution but reactive toward nucleophilic attack.

Uses

1,3,4-Thiadiazole, a bioisostere of the thiazole ring, has been used in the synthesis of cephalosporine and cefazedone, which are used as antibiotics. Megazole is another 1,3,4-thiadiazole-based drug, widely used in the treatment of African trypanosomes, also known as sleeping sickness. Azetepa, a phosphoruscontaining drug, has been used for the treatment of cancer. Tebtheuron is known as a broad-spectrum herbicide and is used to control a variety of weeds and herbaceous and woody plants. Numerous thiadiazole derivatives are patented as bactericides, insecticides, and fungicides.

Definition

ChEBI: 1,3,4-thiadiazole is a thiadiazole.

Chemical Reactivity

Atomic charges have been calculated by the DFT method. The maximum charge was found at the S atom (0.818) and thus it is the favorite position for soft nucleophilic attack. The atomic charge on each carbon is ?0.3275. Because of the presence of the two pyridine-like nitrogen atoms in the ring, which make the C2 - and C5 -positions electronically poor, nucleophilic substitution of the leaving groups present at either the C2 - or C5 -position becomes highly facile. However, the atomic charge on N3 and N4 (?0.0308) makes them preferential sites for electrophilic attack and readily N-alkylated or N-acylated. In strongly basic conditions the thiadiazole ring leads to ring fission.

Biological Activity

Anti-inflammatory,antivira and antimicrobial.

1,3,4-Thiadiazole Preparation Products And Raw materials

Raw materials

Preparation Products

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1,3,4-Thiadiazole Suppliers

Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.
Tel
025-66028182 18626450290
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yftan@aikonchem.com
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China
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16679
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50
Shanghai Haozhixiang Biotechnology Co., Ltd
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526763801 13301653310
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+86-21-51619052
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526763801@qq.com
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Taizhou Changyuan Chemical Technology Co., Ltd.
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15005869072
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tzcyhxkj@163.com
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507
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JinOu Biomedical (Nanjing) Co., Ltd.
Tel
13000000000
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jinoupharma@163
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jinoupharma@163.com
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China
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11721
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58
Guangzhou Austine Biotechnology Co., LTD
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17727342298
Email
2781109436@qq.com
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China
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2003
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Shanghai Maclean Biochemical Technology Co., LTD
Tel
021-021-50706066 15221275939
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China
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Henan Vcommend Consultrading Co., Ltd.
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13393721940
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sales@vcommend.com
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Guangdong Shengke Biochemical Technology Co., Ltd.
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18925112370 18925113981
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Guangdong Wengjiang Chemical Reagent Co.,Ltd.
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0751-2815983 13927872582
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0751-2886750
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2787852318@qq.com
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Ningbo Chaoming Biotechnology Co., Ltd
Tel
13301662590
Email
mandy@atkchemical.com
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China
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