Cas 135382-99-9,(4-Chloro-phenoxy)-thioacetic acid S-(5-methyl-[1,3,4]thiadiazol-2-yl) ester

135382-99-9

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Basic information

Product Name: (4-Chloro-phenoxy)-thioacetic acid S-(5-methyl-[1,3,4]thiadiazol-2-yl) ester
Synonyms: (4-Chloro-phenoxy)-thioacetic acid S-(5-methyl-[1,3,4]thiadiazol-2-yl) ester
CAS NO:135382-99-9
Molecular Formula:
Molecular Weight: 300.79
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (4-Chloro-phenoxy)-thioacetic acid S-(5-methyl-[1,3,4]thiadiazol-2-yl) ester(CAS DataBase Reference)
NIST Chemistry Reference: (4-Chloro-phenoxy)-thioacetic acid S-(5-methyl-[1,3,4]thiadiazol-2-yl) ester(135382-99-9)
EPA Substance Registry System: (4-Chloro-phenoxy)-thioacetic acid S-(5-methyl-[1,3,4]thiadiazol-2-yl) ester(135382-99-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 135382-99-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 135382-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,3,8 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 135382-99:
(8*1)+(7*3)+(6*5)+(5*3)+(4*8)+(3*2)+(2*9)+(1*9)=139
139 % 10 = 9
So 135382-99-9 is a valid CAS Registry Number.

135382-99-9Upstream product

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135382-99-9Relevant academic research and scientific papers

SUGAR CHEMISTRY WITHOUT PROTECTING GROUPS-III. A FACILE CHEMICAL SYNTHESIS OF 6-O-ACYL-D-GLYCOPYRANOSES AND METHYL-6-O-ACYL-D-GLYCOPYRANOSIDES.

Baczko, Krystyna,Plusquellec, Daniel

, p. 3817 - 3828 (2007/10/02)

Regioselective acylation of non protected glycopyranosides was performed using 3-acylthiazolidine-2-thiones 1 and the novel 3-acyl-5-methyl-1,3,4-thiadiazole-2(3H)-thiones 2 as the acylating reagents, yielding 6-O-acylated derivatives in high yields.Acyla

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