Cas 95305-13-8,1H-Pyrrole-2,5-dicarboxylic acid, 3-ethyl-4-methyl-, 5-(1,1-dimethylethyl) 2-methyl ester

95305-13-8

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Basic information

Product Name: 1H-Pyrrole-2,5-dicarboxylic acid, 3-ethyl-4-methyl-, 5-(1,1-dimethylethyl) 2-methyl ester
Synonyms:
CAS NO:95305-13-8
Molecular Formula: C14H21NO4
Molecular Weight: 267.325
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: 1H-Pyrrole-2,5-dicarboxylic acid, 3-ethyl-4-methyl-, 5-(1,1-dimethylethyl) 2-methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Pyrrole-2,5-dicarboxylic acid, 3-ethyl-4-methyl-, 5-(1,1-dimethylethyl) 2-methyl ester(95305-13-8)
EPA Substance Registry System: 1H-Pyrrole-2,5-dicarboxylic acid, 3-ethyl-4-methyl-, 5-(1,1-dimethylethyl) 2-methyl ester(95305-13-8)

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: 95305-13-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 95305-13-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,3,0 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 95305-13:
(7*9)+(6*5)+(5*3)+(4*0)+(3*5)+(2*1)+(1*3)=128
128 % 10 = 8
So 95305-13-8 is a valid CAS Registry Number.

95305-13-8Upstream product

532-31-0 silver benzoate

95305-13-8Downstream Products

95305-13-8Relevant academic research and scientific papers

Synthetic Studies Relevant to Biosynthetic Research on Vitamin B12. Part 2. Syntheses of C-Methylated Chlorins Via Lactams

Battersby, Alan R.,Fookes, Christopher J. R.,Snow, Roger J.

, p. 2733 - 2741 (2007/10/02)

C-Metylyted chlorins have been synthesised by two approaches.For one, ring-B and ring-C of the final chlorin were built sequentially onto a thiolactam system which acted as the A-D component.The preferred alternative method involved joining together a lac

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